Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 4660

1.

rs1491582693 has merged into rs774226017 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA [Show Flanks]
    Chromosome:
    16:15301951 (GRCh38)
    16:15395808 (GRCh37)
    Canonical SPDI:
    NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000016.10:15301938:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
    Gene:
    LOC105371097 (Varview)
    Functional Consequence:
    2KB_upstream_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAAAAAAAAAAAA=0./0 (ALFA)
    HGVS:
    2.

    rs1491578277 [Homo sapiens]
      Variant type:
      INS
      Alleles:
      ->C [Show Flanks]
      Chromosome:
      16:15292081 (GRCh38)
      16:15385939 (GRCh37)
      Canonical SPDI:
      NC_000016.10:15292081::C
      Gene:
      LOC105371097 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency
      MAF:
      C=0.00096/16 (TOMMO)
      HGVS:
      3.

      rs1491442016 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        AA>-,A,AAA [Show Flanks]
        Chromosome:
        16:15292030 (GRCh38)
        16:15385887 (GRCh37)
        Canonical SPDI:
        NC_000016.10:15292028:AAA:A,NC_000016.10:15292028:AAA:AA,NC_000016.10:15292028:AAA:AAAA
        Gene:
        LOC105371097 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0.000061/1 (ALFA)
        -=0.000118/13 (GnomAD)
        -=0.00024/4 (TOMMO)
        HGVS:
        4.

        rs1491433008 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          AA>- [Show Flanks]
          Chromosome:
          16:15292082 (GRCh38)
          16:15385939 (GRCh37)
          Canonical SPDI:
          NC_000016.10:15292080:AAA:A
          Gene:
          LOC105371097 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          -=0.000004/1 (TOPMED)
          -=0.000051/7 (GnomAD)
          -=0.000179/3 (TOMMO)
          HGVS:
          5.

          rs1491416445 [Homo sapiens]
            Variant type:
            INS
            Alleles:
            ->C [Show Flanks]
            Chromosome:
            16:15292029 (GRCh38)
            16:15385887 (GRCh37)
            Canonical SPDI:
            NC_000016.10:15292029::C
            Gene:
            LOC105371097 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency
            MAF:
            C=0.00018/3 (TOMMO)
            HGVS:
            6.

            rs1491402438 has merged into rs753878694 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              TTTTTTTTTT>-,T,TT,TTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT [Show Flanks]
              Chromosome:
              16:15294099 (GRCh38)
              16:15387956 (GRCh37)
              Canonical SPDI:
              NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15294090:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
              Gene:
              LOC105371097 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              TTTTTTTT=0./0 (ALFA)
              -=0.000042/11 (TOPMED)
              HGVS:
              NC_000016.10:g.15294099_15294108del, NC_000016.10:g.15294100_15294108del, NC_000016.10:g.15294101_15294108del, NC_000016.10:g.15294102_15294108del, NC_000016.10:g.15294105_15294108del, NC_000016.10:g.15294106_15294108del, NC_000016.10:g.15294107_15294108del, NC_000016.10:g.15294108del, NC_000016.10:g.15294108dup, NC_000016.10:g.15294107_15294108dup, NC_000016.10:g.15294106_15294108dup, NC_000016.10:g.15294105_15294108dup, NC_000016.10:g.15294104_15294108dup, NC_000016.10:g.15294103_15294108dup, NC_000016.10:g.15294099_15294108dup, NC_000016.9:g.15387956_15387965del, NC_000016.9:g.15387957_15387965del, NC_000016.9:g.15387958_15387965del, NC_000016.9:g.15387959_15387965del, NC_000016.9:g.15387962_15387965del, NC_000016.9:g.15387963_15387965del, NC_000016.9:g.15387964_15387965del, NC_000016.9:g.15387965del, NC_000016.9:g.15387965dup, NC_000016.9:g.15387964_15387965dup, NC_000016.9:g.15387963_15387965dup, NC_000016.9:g.15387962_15387965dup, NC_000016.9:g.15387961_15387965dup, NC_000016.9:g.15387960_15387965dup, NC_000016.9:g.15387956_15387965dup, NT_187607.1:g.368465_368474del, NT_187607.1:g.368466_368474del, NT_187607.1:g.368467_368474del, NT_187607.1:g.368468_368474del, NT_187607.1:g.368471_368474del, NT_187607.1:g.368472_368474del, NT_187607.1:g.368473_368474del, NT_187607.1:g.368474del, NT_187607.1:g.368474dup, NT_187607.1:g.368473_368474dup, NT_187607.1:g.368472_368474dup, NT_187607.1:g.368471_368474dup, NT_187607.1:g.368470_368474dup, NT_187607.1:g.368469_368474dup, NT_187607.1:g.368465_368474dup
              7.

              rs1491370094 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->G [Show Flanks]
                Chromosome:
                16:15285835 (GRCh38)
                16:15379693 (GRCh37)
                Canonical SPDI:
                NC_000016.10:15285835:G:GG
                Gene:
                LOC105371097 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                GG=0./0 (ALFA)
                G=0.000004/1 (TOPMED)
                HGVS:
                8.

                rs1491344580 has merged into rs532538032 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  TTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT [Show Flanks]
                  Chromosome:
                  16:15302424 (GRCh38)
                  16:15396281 (GRCh37)
                  Canonical SPDI:
                  NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000016.10:15302412:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT
                  Gene:
                  LOC105371097 (Varview)
                  Functional Consequence:
                  2KB_upstream_variant,upstream_transcript_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  TTTTTTTTTTTTT=0./0 (ALFA)
                  -=0.125/5 (GENOME_DK)
                  -=0.3878/1942 (1000Genomes)
                  HGVS:
                  NC_000016.10:g.15302424_15302433del, NC_000016.10:g.15302426_15302433del, NC_000016.10:g.15302427_15302433del, NC_000016.10:g.15302428_15302433del, NC_000016.10:g.15302429_15302433del, NC_000016.10:g.15302430_15302433del, NC_000016.10:g.15302431_15302433del, NC_000016.10:g.15302432_15302433del, NC_000016.10:g.15302433del, NC_000016.10:g.15302433dup, NC_000016.10:g.15302432_15302433dup, NC_000016.10:g.15302431_15302433dup, NC_000016.10:g.15302430_15302433dup, NC_000016.10:g.15302429_15302433dup, NC_000016.10:g.15302428_15302433dup, NC_000016.10:g.15302427_15302433dup, NC_000016.9:g.15396281_15396290del, NC_000016.9:g.15396283_15396290del, NC_000016.9:g.15396284_15396290del, NC_000016.9:g.15396285_15396290del, NC_000016.9:g.15396286_15396290del, NC_000016.9:g.15396287_15396290del, NC_000016.9:g.15396288_15396290del, NC_000016.9:g.15396289_15396290del, NC_000016.9:g.15396290del, NC_000016.9:g.15396290dup, NC_000016.9:g.15396289_15396290dup, NC_000016.9:g.15396288_15396290dup, NC_000016.9:g.15396287_15396290dup, NC_000016.9:g.15396286_15396290dup, NC_000016.9:g.15396285_15396290dup, NC_000016.9:g.15396284_15396290dup, NT_187607.1:g.360141_360150del, NT_187607.1:g.360143_360150del, NT_187607.1:g.360144_360150del, NT_187607.1:g.360145_360150del, NT_187607.1:g.360146_360150del, NT_187607.1:g.360147_360150del, NT_187607.1:g.360148_360150del, NT_187607.1:g.360149_360150del, NT_187607.1:g.360150del, NT_187607.1:g.360150dup, NT_187607.1:g.360149_360150dup, NT_187607.1:g.360148_360150dup, NT_187607.1:g.360147_360150dup, NT_187607.1:g.360146_360150dup, NT_187607.1:g.360145_360150dup, NT_187607.1:g.360144_360150dup
                  9.

                  rs1491304964 [Homo sapiens]
                    Variant type:
                    SNV:
                    Alleles:
                    ->G
                    Chromosome:
                    no mapping
                    Canonical SPDI:
                    10.

                    rs1491304580 [Homo sapiens]
                      Variant type:
                      DEL
                      Alleles:
                      CA>- [Show Flanks]
                      Chromosome:
                      16:15301938 (GRCh38)
                      16:15395795 (GRCh37)
                      Canonical SPDI:
                      NC_000016.10:15301937:CA:
                      Gene:
                      LOC105371097 (Varview)
                      Functional Consequence:
                      upstream_transcript_variant,2KB_upstream_variant
                      Validated:
                      by frequency,by alfa
                      MAF:
                      -=0./0 (ALFA)
                      HGVS:
                      11.

                      rs1491213255 [Homo sapiens]
                        Variant type:
                        SNV:
                        Alleles:
                        ->CTT
                        Chromosome:
                        no mapping
                        Canonical SPDI:
                        12.

                        rs1491206795 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          CT>- [Show Flanks]
                          Chromosome:
                          16:15302412 (GRCh38)
                          16:15396269 (GRCh37)
                          Canonical SPDI:
                          NC_000016.10:15302411:CT:
                          Gene:
                          LOC105371097 (Varview)
                          Functional Consequence:
                          upstream_transcript_variant,2KB_upstream_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          -=0./0 (ALFA)
                          HGVS:
                          13.

                          rs1491192595 has merged into rs562733701 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            AA>- [Show Flanks]
                            Chromosome:
                            16:15285770 (GRCh38)
                            16:15379627 (GRCh37)
                            Canonical SPDI:
                            NC_000016.10:15285768:AAA:A
                            Gene:
                            LOC105371097 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by cluster
                            MAF:
                            -=0.015/13 (GnomAD)
                            HGVS:
                            14.

                            rs1491168084 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              AA>-,AAAA [Show Flanks]
                              Chromosome:
                              16:15292058 (GRCh38)
                              16:15385915 (GRCh37)
                              Canonical SPDI:
                              NC_000016.10:15292056:AAA:A,NC_000016.10:15292056:AAA:AAAAA
                              Gene:
                              LOC105371097 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              AAAAA=0./0 (ALFA)
                              -=0.001333/22 (TOMMO)
                              -=0.003401/2 (NorthernSweden)
                              -=0.003704/6 (Korea1K)
                              -=0.010593/1212 (GnomAD)
                              -=0.070388/261 (TWINSUK)
                              -=0.075246/290 (ALSPAC)
                              HGVS:
                              15.

                              rs1491020418 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                ->AA [Show Flanks]
                                Chromosome:
                                16:15285738 (GRCh38)
                                16:15379596 (GRCh37)
                                Canonical SPDI:
                                NC_000016.10:15285738:AAA:AAAAA
                                Gene:
                                LOC105371097 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                AAAAA=0./0 (ALFA)
                                AA=0.000004/1 (TOPMED)
                                HGVS:
                                16.

                                rs1490937086 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  A>C [Show Flanks]
                                  Chromosome:
                                  16:15282576 (GRCh38)
                                  16:15376433 (GRCh37)
                                  Canonical SPDI:
                                  NC_000016.10:15282575:A:C
                                  Gene:
                                  LOC105371097 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  C=0./0 (ALFA)
                                  HGVS:
                                  17.

                                  rs1490927468 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    16:15296590 (GRCh38)
                                    16:15390447 (GRCh37)
                                    Canonical SPDI:
                                    NC_000016.10:15296589:C:T
                                    Gene:
                                    LOC105371097 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000022/3 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1490558859 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      16:15301104 (GRCh38)
                                      16:15394961 (GRCh37)
                                      Canonical SPDI:
                                      NC_000016.10:15301103:A:G
                                      Gene:
                                      LOC105371097 (Varview)
                                      Functional Consequence:
                                      upstream_transcript_variant,2KB_upstream_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000008/2 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1490444962 [Homo sapiens]
                                        Variant type:
                                        DEL
                                        Alleles:
                                        C>- [Show Flanks]
                                        Chromosome:
                                        16:15281940 (GRCh38)
                                        16:15375797 (GRCh37)
                                        Canonical SPDI:
                                        NC_000016.10:15281939:C:
                                        Gene:
                                        LOC105371097 (Varview)
                                        Functional Consequence:
                                        downstream_transcript_variant,500B_downstream_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        -=0./0 (ALFA)
                                        -=0.000004/1 (TOPMED)
                                        -=0.00002/2 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1490388272 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>C [Show Flanks]
                                          Chromosome:
                                          16:15294149 (GRCh38)
                                          16:15388006 (GRCh37)
                                          Canonical SPDI:
                                          NC_000016.10:15294148:T:C
                                          Gene:
                                          LOC105371097 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          C=0./0 (ALFA)
                                          HGVS:

                                          Display Settings:

                                          Format
                                          Items per page
                                          Sort by

                                          Send to:

                                          Choose Destination

                                          Supplemental Content

                                          Find related data

                                          Recent activity

                                          Your browsing activity is empty.

                                          Activity recording is turned off.

                                          Turn recording back on

                                          See more...
                                          Support Center