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1.

rs1491585216 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AA>- [Show Flanks]
    Chromosome:
    16:15111158 (GRCh38)
    16:15205015 (GRCh37)
    Canonical SPDI:
    NC_000016.10:15111155:AAAA:AA
    Gene:
    PDXDC1 (Varview), PKD1P6-NPIPP1 (Varview)
    Functional Consequence:
    intron_variant,genic_downstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAA=0.000084/1 (ALFA)
    -=0.000052/6 (GnomAD)
    HGVS:
    2.

    rs1491560431 has merged into rs1293604743 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      T>-,TT [Show Flanks]
      Chromosome:
      16:15038506 (GRCh38)
      16:15132363 (GRCh37)
      Canonical SPDI:
      NC_000016.10:15038505:TTTTTTT:TTTTTT,NC_000016.10:15038505:TTTTTTT:TTTTTTTT
      Gene:
      PDXDC1 (Varview), NTAN1 (Varview)
      Functional Consequence:
      intron_variant,downstream_transcript_variant,genic_downstream_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      TTTTTTTT=0.000054/1 (ALFA)
      -=0.000021/3 (GnomAD)
      -=0.000223/1 (Estonian)
      HGVS:
      3.

      rs1491541645 has merged into rs66850292 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        ACACACACACACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACACACACAC [Show Flanks]
        Chromosome:
        16:15020988 (GRCh38)
        16:15114845 (GRCh37)
        Canonical SPDI:
        NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000016.10:15020975:ACACACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACAC
        Gene:
        PDXDC1 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        ACACACACACAC=0./0 (ALFA)
        AC=0.3025/1515 (1000Genomes)
        HGVS:
        NC_000016.10:g.15020976AC[6], NC_000016.10:g.15020976AC[7], NC_000016.10:g.15020976AC[8], NC_000016.10:g.15020976AC[9], NC_000016.10:g.15020976AC[10], NC_000016.10:g.15020976AC[11], NC_000016.10:g.15020976AC[12], NC_000016.10:g.15020976AC[13], NC_000016.10:g.15020976AC[14], NC_000016.10:g.15020976AC[15], NC_000016.10:g.15020976AC[16], NC_000016.10:g.15020976AC[17], NC_000016.10:g.15020976AC[19], NC_000016.10:g.15020976AC[20], NC_000016.10:g.15020976AC[21], NC_000016.10:g.15020976AC[22], NC_000016.10:g.15020976AC[23], NC_000016.10:g.15020976AC[24], NC_000016.10:g.15020976AC[25], NC_000016.10:g.15020976AC[26], NC_000016.10:g.15020976AC[27], NC_000016.10:g.15020976AC[28], NC_000016.10:g.15020976AC[29], NC_000016.9:g.15114833AC[6], NC_000016.9:g.15114833AC[7], NC_000016.9:g.15114833AC[8], NC_000016.9:g.15114833AC[9], NC_000016.9:g.15114833AC[10], NC_000016.9:g.15114833AC[11], NC_000016.9:g.15114833AC[12], NC_000016.9:g.15114833AC[13], NC_000016.9:g.15114833AC[14], NC_000016.9:g.15114833AC[15], NC_000016.9:g.15114833AC[16], NC_000016.9:g.15114833AC[17], NC_000016.9:g.15114833AC[19], NC_000016.9:g.15114833AC[20], NC_000016.9:g.15114833AC[21], NC_000016.9:g.15114833AC[22], NC_000016.9:g.15114833AC[23], NC_000016.9:g.15114833AC[24], NC_000016.9:g.15114833AC[25], NC_000016.9:g.15114833AC[26], NC_000016.9:g.15114833AC[27], NC_000016.9:g.15114833AC[28], NC_000016.9:g.15114833AC[29], NT_187607.1:g.860318AC[7], NT_187607.1:g.860318AC[8], NT_187607.1:g.860318AC[9], NT_187607.1:g.860318AC[10], NT_187607.1:g.860318AC[11], NT_187607.1:g.860318AC[12], NT_187607.1:g.860318AC[13], NT_187607.1:g.860318AC[14], NT_187607.1:g.860318AC[15], NT_187607.1:g.860318AC[16], NT_187607.1:g.860318AC[17], NT_187607.1:g.860318AC[18], NT_187607.1:g.860318AC[20], NT_187607.1:g.860318AC[21], NT_187607.1:g.860318AC[22], NT_187607.1:g.860318AC[23], NT_187607.1:g.860318AC[24], NT_187607.1:g.860318AC[25], NT_187607.1:g.860318AC[26], NT_187607.1:g.860318AC[27], NT_187607.1:g.860318AC[28], NT_187607.1:g.860318AC[29], NT_187607.1:g.860318AC[30]
        4.

        rs1491528358 has merged into rs71278923 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AAA>-,A,AA,AAAA,AAAAA,AAAAAA [Show Flanks]
          Chromosome:
          16:15015728 (GRCh38)
          16:15109585 (GRCh37)
          Canonical SPDI:
          NC_000016.10:15015715:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:15015715:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:15015715:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:15015715:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:15015715:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:15015715:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA
          Gene:
          PDXDC1 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          AAAAAAAAAAAAA=0./0 (ALFA)
          HGVS:
          5.

          rs1491516213 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            ->G [Show Flanks]
            Chromosome:
            16:14985994 (GRCh38)
            16:15079852 (GRCh37)
            Canonical SPDI:
            NC_000016.10:14985994:GGGGG:GGGGGG
            Gene:
            PDXDC1 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            GGGGGG=0./0 (ALFA)
            G=0.000021/3 (GnomAD)
            HGVS:
            6.

            rs1491515223 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTT>-,T,TTTTT [Show Flanks]
              Chromosome:
              16:15058439 (GRCh38)
              16:15152296 (GRCh37)
              Canonical SPDI:
              NC_000016.10:15058436:TTTTTT:TT,NC_000016.10:15058436:TTTTTT:TTT,NC_000016.10:15058436:TTTTTT:TTTTTTT
              Gene:
              PDXDC1 (Varview)
              Functional Consequence:
              intron_variant,genic_downstream_transcript_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTT=0./0 (ALFA)
              T=0.000064/9 (GnomAD)
              HGVS:
              7.

              rs1491498997 [Homo sapiens]
                Variant type:
                SNV:
                Alleles:
                CA>-
                Chromosome:
                no mapping
                Canonical SPDI:
                8.

                rs1491480174 [Homo sapiens]
                  Variant type:
                  INS
                  Alleles:
                  ->G [Show Flanks]
                  Chromosome:
                  16:15013360 (GRCh38)
                  16:15107218 (GRCh37)
                  Canonical SPDI:
                  NC_000016.10:15013360::G
                  Gene:
                  PDXDC1 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  G=0./0 (ALFA)
                  G=0.00001/1 (GnomAD)
                  HGVS:
                  9.

                  rs1491479793 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    ->C [Show Flanks]
                    Chromosome:
                    16:15089811 (GRCh38)
                    16:15183669 (GRCh37)
                    Canonical SPDI:
                    NC_000016.10:15089811:C:CC
                    Gene:
                    PDXDC1 (Varview), RRN3 (Varview)
                    Functional Consequence:
                    intron_variant,genic_downstream_transcript_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    CC=0./0 (ALFA)
                    C=0.005431/668 (GnomAD)
                    HGVS:
                    10.

                    rs1491473989 [Homo sapiens]
                      Variant type:
                      DEL
                      Alleles:
                      CA>- [Show Flanks]
                      Chromosome:
                      16:15116479 (GRCh38)
                      16:15210336 (GRCh37)
                      Canonical SPDI:
                      NC_000016.10:15116478:CA:
                      Gene:
                      PDXDC1 (Varview), PKD1P6-NPIPP1 (Varview)
                      Functional Consequence:
                      intron_variant,genic_downstream_transcript_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      -=0.00042/5 (ALFA)
                      HGVS:
                      11.

                      rs1491472512 [Homo sapiens]
                        Variant type:
                        DEL
                        Alleles:
                        CA>- [Show Flanks]
                        Chromosome:
                        16:15046697 (GRCh38)
                        16:15140554 (GRCh37)
                        Canonical SPDI:
                        NC_000016.10:15046696:CA:
                        Gene:
                        PDXDC1 (Varview), NTAN1 (Varview)
                        Functional Consequence:
                        intron_variant,genic_upstream_transcript_variant,genic_downstream_transcript_variant,upstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        -=0.00025/3 (ALFA)
                        HGVS:
                        13.

                        rs1491447042 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          CA>- [Show Flanks]
                          Chromosome:
                          16:15089786 (GRCh38)
                          16:15183643 (GRCh37)
                          Canonical SPDI:
                          NC_000016.10:15089785:CA:
                          Gene:
                          PDXDC1 (Varview), RRN3 (Varview)
                          Functional Consequence:
                          intron_variant,genic_downstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0.00051/6 (ALFA)
                          HGVS:
                          14.

                          rs1491435794 has merged into rs11421981 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
                            Chromosome:
                            16:14997741 (GRCh38)
                            16:15091598 (GRCh37)
                            Canonical SPDI:
                            NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:14997732:TTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
                            Gene:
                            PDXDC1 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTTTTTTTTTTTT=0.00021/3 (ALFA)
                            -=0.0088/27 (1000Genomes)
                            -=0.4/16 (GENOME_DK)
                            HGVS:
                            NC_000016.10:g.14997741_14997743del, NC_000016.10:g.14997742_14997743del, NC_000016.10:g.14997743del, NC_000016.10:g.14997743dup, NC_000016.10:g.14997742_14997743dup, NC_000016.10:g.14997741_14997743dup, NC_000016.10:g.14997740_14997743dup, NC_000016.10:g.14997739_14997743dup, NC_000016.10:g.14997743_14997744insTTTTTTTTTTTTT, NC_000016.9:g.15091598_15091600del, NC_000016.9:g.15091599_15091600del, NC_000016.9:g.15091600del, NC_000016.9:g.15091600dup, NC_000016.9:g.15091599_15091600dup, NC_000016.9:g.15091598_15091600dup, NC_000016.9:g.15091597_15091600dup, NC_000016.9:g.15091596_15091600dup, NC_000016.9:g.15091600_15091601insTTTTTTTTTTTTT, NT_187607.1:g.837088_837090del, NT_187607.1:g.837089_837090del, NT_187607.1:g.837090del, NT_187607.1:g.837090dup, NT_187607.1:g.837089_837090dup, NT_187607.1:g.837088_837090dup, NT_187607.1:g.837087_837090dup, NT_187607.1:g.837086_837090dup, NT_187607.1:g.837090_837091insTTTTTTTTTTTTT
                            15.

                            rs1491424727 has merged into rs1162300755 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              TTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT [Show Flanks]
                              Chromosome:
                              16:15126666 (GRCh38)
                              16:15220523 (GRCh37)
                              Canonical SPDI:
                              NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:15126655:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
                              Gene:
                              PDXDC1 (Varview), PKD1P6-NPIPP1 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              TTTTTTTTTTTTTT=0./0 (ALFA)
                              HGVS:
                              NC_000016.10:g.15126666_15126673del, NC_000016.10:g.15126668_15126673del, NC_000016.10:g.15126670_15126673del, NC_000016.10:g.15126671_15126673del, NC_000016.10:g.15126672_15126673del, NC_000016.10:g.15126673del, NC_000016.10:g.15126673dup, NC_000016.10:g.15126672_15126673dup, NC_000016.10:g.15126671_15126673dup, NC_000016.9:g.15220523_15220530del, NC_000016.9:g.15220525_15220530del, NC_000016.9:g.15220527_15220530del, NC_000016.9:g.15220528_15220530del, NC_000016.9:g.15220529_15220530del, NC_000016.9:g.15220530del, NC_000016.9:g.15220530dup, NC_000016.9:g.15220529_15220530dup, NC_000016.9:g.15220528_15220530dup, NG_002799.5:g.28311_28318del, NG_002799.5:g.28313_28318del, NG_002799.5:g.28315_28318del, NG_002799.5:g.28316_28318del, NG_002799.5:g.28317_28318del, NG_002799.5:g.28318del, NG_002799.5:g.28318dup, NG_002799.5:g.28317_28318dup, NG_002799.5:g.28316_28318dup, NT_187607.1:g.538592_538599del, NT_187607.1:g.538594_538599del, NT_187607.1:g.538596_538599del, NT_187607.1:g.538597_538599del, NT_187607.1:g.538598_538599del, NT_187607.1:g.538599del, NT_187607.1:g.538599dup, NT_187607.1:g.538598_538599dup, NT_187607.1:g.538597_538599dup
                              16.

                              rs1491389896 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                CT>- [Show Flanks]
                                Chromosome:
                                16:15007157 (GRCh38)
                                16:15101014 (GRCh37)
                                Canonical SPDI:
                                NC_000016.10:15007156:CT:
                                Gene:
                                PDXDC1 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                -=0./0 (ALFA)
                                HGVS:
                                17.

                                rs1491380278 has merged into rs779875897 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
                                  Chromosome:
                                  16:15013371 (GRCh38)
                                  16:15107228 (GRCh37)
                                  Canonical SPDI:
                                  NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:15013359:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
                                  Gene:
                                  PDXDC1 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  AAAAAAAAAAAA=0./0 (ALFA)
                                  HGVS:
                                  18.

                                  rs1491368472 has merged into rs766580023 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    AAAAAA>-,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA [Show Flanks]
                                    Chromosome:
                                    16:15113233 (GRCh38)
                                    16:15207090 (GRCh37)
                                    Canonical SPDI:
                                    NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:15113222:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
                                    Gene:
                                    PDXDC1 (Varview), PKD1P6-NPIPP1 (Varview)
                                    Functional Consequence:
                                    genic_downstream_transcript_variant,intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    AAAAAAAAAAAAA=0./0 (ALFA)
                                    A=0.3947/15 (GENOME_DK)
                                    HGVS:
                                    NC_000016.10:g.15113233_15113238del, NC_000016.10:g.15113236_15113238del, NC_000016.10:g.15113237_15113238del, NC_000016.10:g.15113238del, NC_000016.10:g.15113238dup, NC_000016.10:g.15113237_15113238dup, NC_000016.10:g.15113236_15113238dup, NC_000016.9:g.15207090_15207095del, NC_000016.9:g.15207093_15207095del, NC_000016.9:g.15207094_15207095del, NC_000016.9:g.15207095del, NC_000016.9:g.15207095dup, NC_000016.9:g.15207094_15207095dup, NC_000016.9:g.15207093_15207095dup, NG_032198.4:g.10371_10376del, NG_032198.4:g.10374_10376del, NG_032198.4:g.10375_10376del, NG_032198.4:g.10376del, NG_032198.4:g.10376dup, NG_032198.4:g.10375_10376dup, NG_032198.4:g.10374_10376dup, NT_187607.1:g.552038_552043del, NT_187607.1:g.552041_552043del, NT_187607.1:g.552042_552043del, NT_187607.1:g.552043del, NT_187607.1:g.552043dup, NT_187607.1:g.552042_552043dup, NT_187607.1:g.552041_552043dup
                                    19.

                                    rs1491367237 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      ->T [Show Flanks]
                                      Chromosome:
                                      16:15057423 (GRCh38)
                                      16:15151281 (GRCh37)
                                      Canonical SPDI:
                                      NC_000016.10:15057423:T:TT
                                      Gene:
                                      PDXDC1 (Varview), NTAN1 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_downstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TT=0./0 (ALFA)
                                      T=0.000004/1 (TOPMED)
                                      T=0.000007/1 (GnomAD)
                                      HGVS:
                                      20.

                                      rs1491360987 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        ->G [Show Flanks]
                                        Chromosome:
                                        16:15013358 (GRCh38)
                                        16:15107216 (GRCh37)
                                        Canonical SPDI:
                                        NC_000016.10:15013358:G:GG
                                        Gene:
                                        PDXDC1 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        GG=0./0 (ALFA)
                                        G=0.000022/3 (GnomAD)
                                        HGVS:

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