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Items: 1 to 20 of 1188

1.

rs1490883209 [Homo sapiens]
    Variant type:
    SNV
    Alleles:
    G>C [Show Flanks]
    Chromosome:
    4:74097376 (GRCh38)
    4:74963093 (GRCh37)
    Canonical SPDI:
    NC_000004.12:74097375:G:C
    Gene:
    CXCL2 (Varview)
    Functional Consequence:
    3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    C=0./0 (ALFA)
    C=0.000004/1 (TOPMED)
    C=0.000007/1 (GnomAD)
    HGVS:
    2.

    rs1490878004 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      A>- [Show Flanks]
      Chromosome:
      4:74098634 (GRCh38)
      4:74964351 (GRCh37)
      Canonical SPDI:
      NC_000004.12:74098633:A:
      Gene:
      CXCL2 (Varview)
      Functional Consequence:
      frameshift_variant,coding_sequence_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      -=0./0 (ALFA)
      -=0.000007/1 (GnomAD)
      -=0.000008/2 (TOPMED)
      HGVS:
      3.

      rs1490388877 [Homo sapiens]
        Variant type:
        SNV
        Alleles:
        G>A,T [Show Flanks]
        Chromosome:
        4:74098028 (GRCh38)
        4:74963745 (GRCh37)
        Canonical SPDI:
        NC_000004.12:74098027:G:A,NC_000004.12:74098027:G:T
        Gene:
        CXCL2 (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        T=0./0 (ALFA)
        A=0.000004/1 (TOPMED)
        HGVS:
        4.

        rs1489960876 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>C,T [Show Flanks]
          Chromosome:
          4:74098971 (GRCh38)
          4:74964688 (GRCh37)
          Canonical SPDI:
          NC_000004.12:74098970:G:C,NC_000004.12:74098970:G:T
          Gene:
          CXCL2 (Varview)
          Functional Consequence:
          intron_variant
          Validated:
          by frequency
          MAF:
          T=0.000005/1 (GnomAD_exomes)
          HGVS:
          5.

          rs1489530937 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            C>T [Show Flanks]
            Chromosome:
            4:74099035 (GRCh38)
            4:74964752 (GRCh37)
            Canonical SPDI:
            NC_000004.12:74099034:C:T
            Gene:
            CXCL2 (Varview)
            Functional Consequence:
            missense_variant,coding_sequence_variant
            Validated:
            by frequency,by cluster
            MAF:
            T=0.00012/2 (TOMMO)
            HGVS:
            6.

            rs1489488754 [Homo sapiens]
              Variant type:
              SNV
              Alleles:
              C>T [Show Flanks]
              Chromosome:
              4:74098977 (GRCh38)
              4:74964694 (GRCh37)
              Canonical SPDI:
              NC_000004.12:74098976:C:T
              Gene:
              CXCL2 (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              T=0./0 (ALFA)
              T=0.000008/2 (TOPMED)
              HGVS:
              7.

              rs1487386351 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ->CCTT [Show Flanks]
                Chromosome:
                4:74097539 (GRCh38)
                4:74963257 (GRCh37)
                Canonical SPDI:
                NC_000004.12:74097539:CCTT:CCTTCCTT
                Gene:
                CXCL2 (Varview)
                Functional Consequence:
                3_prime_UTR_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                CCTTCCTT=0./0 (ALFA)
                CCTT=0.000007/1 (GnomAD)
                CCTT=0.000008/2 (TOPMED)
                HGVS:
                8.

                rs1484830872 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>G [Show Flanks]
                  Chromosome:
                  4:74099243 (GRCh38)
                  4:74964960 (GRCh37)
                  Canonical SPDI:
                  NC_000004.12:74099242:A:G
                  Gene:
                  CXCL2 (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)
                  G=0.000014/2 (GnomAD)
                  HGVS:
                  9.

                  rs1484829074 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>T [Show Flanks]
                    Chromosome:
                    4:74098798 (GRCh38)
                    4:74964515 (GRCh37)
                    Canonical SPDI:
                    NC_000004.12:74098797:C:T
                    Gene:
                    CXCL2 (Varview)
                    Functional Consequence:
                    splice_donor_variant
                    Validated:
                    by frequency
                    MAF:
                    T=0.000004/1 (GnomAD_exomes)
                    HGVS:
                    10.

                    rs1483944534 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      G>T [Show Flanks]
                      Chromosome:
                      4:74100319 (GRCh38)
                      4:74966036 (GRCh37)
                      Canonical SPDI:
                      NC_000004.12:74100318:G:T
                      Gene:
                      CXCL2 (Varview)
                      Functional Consequence:
                      upstream_transcript_variant,2KB_upstream_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      T=0./0 (ALFA)
                      T=0.000004/1 (TOPMED)
                      T=0.000007/1 (GnomAD)
                      HGVS:
                      11.

                      rs1483785831 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        G>A [Show Flanks]
                        Chromosome:
                        4:74099915 (GRCh38)
                        4:74965632 (GRCh37)
                        Canonical SPDI:
                        NC_000004.12:74099914:G:A
                        Gene:
                        CXCL2 (Varview)
                        Functional Consequence:
                        upstream_transcript_variant,2KB_upstream_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        A=0.000071/1 (ALFA)
                        A=0.000014/2 (GnomAD)
                        HGVS:
                        12.

                        rs1482062633 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          4:74100449 (GRCh38)
                          4:74966166 (GRCh37)
                          Canonical SPDI:
                          NC_000004.12:74100448:G:A
                          Gene:
                          CXCL2 (Varview)
                          Functional Consequence:
                          2KB_upstream_variant,upstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000008/2 (TOPMED)
                          HGVS:
                          13.

                          rs1481167194 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A,T [Show Flanks]
                            Chromosome:
                            4:74101142 (GRCh38)
                            4:74966859 (GRCh37)
                            Canonical SPDI:
                            NC_000004.12:74101141:C:A,NC_000004.12:74101141:C:T
                            Gene:
                            CXCL2 (Varview)
                            Functional Consequence:
                            2KB_upstream_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            T=0./0 (ALFA)
                            HGVS:
                            14.

                            rs1481133741 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              A>T [Show Flanks]
                              Chromosome:
                              4:74098447 (GRCh38)
                              4:74964164 (GRCh37)
                              Canonical SPDI:
                              NC_000004.12:74098446:A:T
                              Gene:
                              CXCL2 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              T=0.000071/1 (ALFA)
                              T=0.000007/1 (GnomAD)
                              T=0.000026/7 (TOPMED)
                              HGVS:
                              15.

                              rs1480523200 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                T>A [Show Flanks]
                                Chromosome:
                                4:74098123 (GRCh38)
                                4:74963840 (GRCh37)
                                Canonical SPDI:
                                NC_000004.12:74098122:T:A
                                Gene:
                                CXCL2 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0.000071/1 (ALFA)
                                A=0.000004/1 (TOPMED)
                                HGVS:
                                16.

                                rs1480172569 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  T>C [Show Flanks]
                                  Chromosome:
                                  4:74098342 (GRCh38)
                                  4:74964059 (GRCh37)
                                  Canonical SPDI:
                                  NC_000004.12:74098341:T:C
                                  Gene:
                                  CXCL2 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  C=0./0 (ALFA)
                                  C=0.000004/1 (TOPMED)
                                  HGVS:
                                  17.

                                  rs1480151838 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>G,T [Show Flanks]
                                    Chromosome:
                                    4:74099309 (GRCh38)
                                    4:74965026 (GRCh37)
                                    Canonical SPDI:
                                    NC_000004.12:74099308:C:G,NC_000004.12:74099308:C:T
                                    Gene:
                                    CXCL2 (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000007/1 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1479867757 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      C>A [Show Flanks]
                                      Chromosome:
                                      4:74099052 (GRCh38)
                                      4:74964769 (GRCh37)
                                      Canonical SPDI:
                                      NC_000004.12:74099051:C:A
                                      Gene:
                                      CXCL2 (Varview)
                                      Functional Consequence:
                                      coding_sequence_variant,synonymous_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      A=0./0 (ALFA)
                                      A=0.000004/1 (TOPMED)
                                      HGVS:
                                      19.

                                      rs1479758510 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        A>G [Show Flanks]
                                        Chromosome:
                                        4:74097407 (GRCh38)
                                        4:74963124 (GRCh37)
                                        Canonical SPDI:
                                        NC_000004.12:74097406:A:G
                                        Gene:
                                        CXCL2 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000011/3 (TOPMED)
                                        G=0.000021/3 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1479706276 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>G [Show Flanks]
                                          Chromosome:
                                          4:74099676 (GRCh38)
                                          4:74965393 (GRCh37)
                                          Canonical SPDI:
                                          NC_000004.12:74099675:T:G
                                          Gene:
                                          CXCL2 (Varview)
                                          Functional Consequence:
                                          2KB_upstream_variant,upstream_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          G=0./0 (ALFA)
                                          G=0.000023/6 (TOPMED)
                                          G=0.000036/5 (GnomAD)
                                          HGVS:

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