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Items: 1 to 20 of 1000

1.

rs1491543645 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    ->CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CATACA,CATACACA,CATACACACA,CATACACACACA,CATACACACACACA [Show Flanks]
    Chromosome:
    10:121524099 (GRCh38)
    10:123283614 (GRCh37)
    Canonical SPDI:
    NC_000010.11:121524099:A:ACA,NC_000010.11:121524099:A:ACACA,NC_000010.11:121524099:A:ACACACA,NC_000010.11:121524099:A:ACACACACA,NC_000010.11:121524099:A:ACACACACACA,NC_000010.11:121524099:A:ACACACACACACA,NC_000010.11:121524099:A:ACACACACACACACA,NC_000010.11:121524099:A:ACATACA,NC_000010.11:121524099:A:ACATACACA,NC_000010.11:121524099:A:ACATACACACA,NC_000010.11:121524099:A:ACATACACACACA,NC_000010.11:121524099:A:ACATACACACACACA
    Gene:
    FGFR2 (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ACACA=0./0 (ALFA)
    HGVS:
    NC_000010.11:g.121524100_121524101insCA, NC_000010.11:g.121524100_121524101insCACA, NC_000010.11:g.121524101CA[3], NC_000010.11:g.121524101CA[4], NC_000010.11:g.121524101CA[5], NC_000010.11:g.121524101CA[6], NC_000010.11:g.121524101CA[7], NC_000010.11:g.121524100_121524101insCATACA, NC_000010.11:g.121524100_121524101insCATACACA, NC_000010.11:g.121524100_121524101insCATACACACA, NC_000010.11:g.121524100_121524101insCATACACACACA, NC_000010.11:g.121524100_121524101insCATACACACACACA, NC_000010.10:g.123283614_123283615insCA, NC_000010.10:g.123283614_123283615insCACA, NC_000010.10:g.123283615CA[3], NC_000010.10:g.123283615CA[4], NC_000010.10:g.123283615CA[5], NC_000010.10:g.123283615CA[6], NC_000010.10:g.123283615CA[7], NC_000010.10:g.123283614_123283615insCATACA, NC_000010.10:g.123283614_123283615insCATACACA, NC_000010.10:g.123283614_123283615insCATACACACA, NC_000010.10:g.123283614_123283615insCATACACACACA, NC_000010.10:g.123283614_123283615insCATACACACACACA, NG_012449.2:g.79359_79360insGT, NG_012449.2:g.79359_79360insGTGT, NG_012449.2:g.79360GT[3], NG_012449.2:g.79360GT[4], NG_012449.2:g.79360GT[5], NG_012449.2:g.79360GT[6], NG_012449.2:g.79360GT[7], NG_012449.2:g.79359_79360insGTATGT, NG_012449.2:g.79359TG[2]TATGT[1], NG_012449.2:g.79359TG[3]TATGT[1], NG_012449.2:g.79359TG[4]TATGT[1], NG_012449.2:g.79359TG[5]TATGT[1]
    2.

    rs1491533428 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      AT>- [Show Flanks]
      Chromosome:
      10:121527592 (GRCh38)
      10:123287106 (GRCh37)
      Canonical SPDI:
      NC_000010.11:121527591:AT:
      Gene:
      FGFR2 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      -=0./0 (ALFA)
      -=0.000035/1 (TOMMO)
      -=0.000053/14 (TOPMED)
      -=0.001032/9 (GnomAD)
      HGVS:
      3.

      rs1491513017 [Homo sapiens]
        Variant type:
        DEL
        Alleles:
        TG>- [Show Flanks]
        Chromosome:
        10:121556434 (GRCh38)
        10:123315948 (GRCh37)
        Canonical SPDI:
        NC_000010.11:121556433:TG:
        Gene:
        FGFR2 (Varview)
        Functional Consequence:
        genic_upstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        -=0./0 (ALFA)
        -=0.00908/35 (ALSPAC)
        -=0.01753/65 (TWINSUK)
        HGVS:
        4.

        rs1491482631 [Homo sapiens]
          Variant type:
          INS
          Alleles:
          ->TC,TCTCTCTCTC,TCTCTCTCTCTCTCTCTCTCTCTCTCTC [Show Flanks]
          Chromosome:
          10:121556395 (GRCh38)
          10:123315910 (GRCh37)
          Canonical SPDI:
          NC_000010.11:121556395::TC,NC_000010.11:121556395::TCTCTCTCTC,NC_000010.11:121556395::TCTCTCTCTCTCTCTCTCTCTCTCTCTC
          Gene:
          FGFR2 (Varview)
          Functional Consequence:
          genic_upstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          TC=0./0 (ALFA)
          TCTCTCTCTCTCTCTCTCTCTCTCTCTC=0.00001/1 (GnomAD)
          HGVS:
          5.

          rs1491461500 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            TA>- [Show Flanks]
            Chromosome:
            10:121556395 (GRCh38)
            10:123315909 (GRCh37)
            Canonical SPDI:
            NC_000010.11:121556394:TA:
            Gene:
            FGFR2 (Varview)
            Functional Consequence:
            genic_upstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            -=0./0 (ALFA)
            HGVS:
            6.

            rs1491386420 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->CCTC [Show Flanks]
              Chromosome:
              10:121556396 (GRCh38)
              10:123315911 (GRCh37)
              Canonical SPDI:
              NC_000010.11:121556396:CTC:CTCCCTC
              Gene:
              FGFR2 (Varview)
              Functional Consequence:
              genic_upstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa
              MAF:
              CTCCCTC=0.000169/2 (ALFA)
              CTCC=0.000026/3 (GnomAD)
              HGVS:
              7.

              rs1491373137 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                GG>- [Show Flanks]
                Chromosome:
                10:121480124 (GRCh38)
                10:123239638 (GRCh37)
                Canonical SPDI:
                NC_000010.11:121480122:GGG:G
                Gene:
                FGFR2 (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa
                MAF:
                G=0.0001/1 (ALFA)
                HGVS:
                8.

                rs1491364101 [Homo sapiens]
                  Variant type:
                  DEL
                  Alleles:
                  CA>- [Show Flanks]
                  Chromosome:
                  10:121488540 (GRCh38)
                  10:123248054 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:121488539:CA:
                  Gene:
                  FGFR2 (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  -=0.00177/21 (ALFA)
                  HGVS:
                  9.

                  rs1491343469 has merged into rs60596436 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                    Chromosome:
                    10:121488550 (GRCh38)
                    10:123248064 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121488540:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                    Gene:
                    FGFR2 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    AAAAAAAAAAAA=0./0 (ALFA)
                    HGVS:
                    NC_000010.11:g.121488550_121488559del, NC_000010.11:g.121488552_121488559del, NC_000010.11:g.121488553_121488559del, NC_000010.11:g.121488554_121488559del, NC_000010.11:g.121488555_121488559del, NC_000010.11:g.121488556_121488559del, NC_000010.11:g.121488557_121488559del, NC_000010.11:g.121488558_121488559del, NC_000010.11:g.121488559del, NC_000010.11:g.121488559dup, NC_000010.11:g.121488558_121488559dup, NC_000010.11:g.121488557_121488559dup, NC_000010.11:g.121488555_121488559dup, NC_000010.11:g.121488552_121488559dup, NC_000010.11:g.121488549_121488559dup, NC_000010.10:g.123248064_123248073del, NC_000010.10:g.123248066_123248073del, NC_000010.10:g.123248067_123248073del, NC_000010.10:g.123248068_123248073del, NC_000010.10:g.123248069_123248073del, NC_000010.10:g.123248070_123248073del, NC_000010.10:g.123248071_123248073del, NC_000010.10:g.123248072_123248073del, NC_000010.10:g.123248073del, NC_000010.10:g.123248073dup, NC_000010.10:g.123248072_123248073dup, NC_000010.10:g.123248071_123248073dup, NC_000010.10:g.123248069_123248073dup, NC_000010.10:g.123248066_123248073dup, NC_000010.10:g.123248063_123248073dup, NG_012449.2:g.114909_114918del, NG_012449.2:g.114911_114918del, NG_012449.2:g.114912_114918del, NG_012449.2:g.114913_114918del, NG_012449.2:g.114914_114918del, NG_012449.2:g.114915_114918del, NG_012449.2:g.114916_114918del, NG_012449.2:g.114917_114918del, NG_012449.2:g.114918del, NG_012449.2:g.114918dup, NG_012449.2:g.114917_114918dup, NG_012449.2:g.114916_114918dup, NG_012449.2:g.114914_114918dup, NG_012449.2:g.114911_114918dup, NG_012449.2:g.114908_114918dup
                    10.

                    rs1491303933 has merged into rs34753296 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                      Chromosome:
                      10:121560625 (GRCh38)
                      10:123320139 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121560615:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                      Gene:
                      FGFR2 (Varview)
                      Functional Consequence:
                      intron_variant,genic_upstream_transcript_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAAAAAAA=0./0 (ALFA)
                      AAAAAAAA=0.0074/4 (NorthernSweden)
                      -=0.4/16 (GENOME_DK)
                      HGVS:
                      NC_000010.11:g.121560625_121560641del, NC_000010.11:g.121560626_121560641del, NC_000010.11:g.121560627_121560641del, NC_000010.11:g.121560628_121560641del, NC_000010.11:g.121560629_121560641del, NC_000010.11:g.121560630_121560641del, NC_000010.11:g.121560631_121560641del, NC_000010.11:g.121560632_121560641del, NC_000010.11:g.121560633_121560641del, NC_000010.11:g.121560634_121560641del, NC_000010.11:g.121560635_121560641del, NC_000010.11:g.121560636_121560641del, NC_000010.11:g.121560637_121560641del, NC_000010.11:g.121560638_121560641del, NC_000010.11:g.121560639_121560641del, NC_000010.11:g.121560640_121560641del, NC_000010.11:g.121560641del, NC_000010.11:g.121560641dup, NC_000010.11:g.121560640_121560641dup, NC_000010.11:g.121560639_121560641dup, NC_000010.11:g.121560638_121560641dup, NC_000010.11:g.121560637_121560641dup, NC_000010.11:g.121560636_121560641dup, NC_000010.11:g.121560635_121560641dup, NC_000010.11:g.121560634_121560641dup, NC_000010.11:g.121560633_121560641dup, NC_000010.11:g.121560632_121560641dup, NC_000010.11:g.121560631_121560641dup, NC_000010.11:g.121560629_121560641dup, NC_000010.10:g.123320139_123320155del, NC_000010.10:g.123320140_123320155del, NC_000010.10:g.123320141_123320155del, NC_000010.10:g.123320142_123320155del, NC_000010.10:g.123320143_123320155del, NC_000010.10:g.123320144_123320155del, NC_000010.10:g.123320145_123320155del, NC_000010.10:g.123320146_123320155del, NC_000010.10:g.123320147_123320155del, NC_000010.10:g.123320148_123320155del, NC_000010.10:g.123320149_123320155del, NC_000010.10:g.123320150_123320155del, NC_000010.10:g.123320151_123320155del, NC_000010.10:g.123320152_123320155del, NC_000010.10:g.123320153_123320155del, NC_000010.10:g.123320154_123320155del, NC_000010.10:g.123320155del, NC_000010.10:g.123320155dup, NC_000010.10:g.123320154_123320155dup, NC_000010.10:g.123320153_123320155dup, NC_000010.10:g.123320152_123320155dup, NC_000010.10:g.123320151_123320155dup, NC_000010.10:g.123320150_123320155dup, NC_000010.10:g.123320149_123320155dup, NC_000010.10:g.123320148_123320155dup, NC_000010.10:g.123320147_123320155dup, NC_000010.10:g.123320146_123320155dup, NC_000010.10:g.123320145_123320155dup, NC_000010.10:g.123320143_123320155dup, NG_012449.2:g.42827_42843del, NG_012449.2:g.42828_42843del, NG_012449.2:g.42829_42843del, NG_012449.2:g.42830_42843del, NG_012449.2:g.42831_42843del, NG_012449.2:g.42832_42843del, NG_012449.2:g.42833_42843del, NG_012449.2:g.42834_42843del, NG_012449.2:g.42835_42843del, NG_012449.2:g.42836_42843del, NG_012449.2:g.42837_42843del, NG_012449.2:g.42838_42843del, NG_012449.2:g.42839_42843del, NG_012449.2:g.42840_42843del, NG_012449.2:g.42841_42843del, NG_012449.2:g.42842_42843del, NG_012449.2:g.42843del, NG_012449.2:g.42843dup, NG_012449.2:g.42842_42843dup, NG_012449.2:g.42841_42843dup, NG_012449.2:g.42840_42843dup, NG_012449.2:g.42839_42843dup, NG_012449.2:g.42838_42843dup, NG_012449.2:g.42837_42843dup, NG_012449.2:g.42836_42843dup, NG_012449.2:g.42835_42843dup, NG_012449.2:g.42834_42843dup, NG_012449.2:g.42833_42843dup, NG_012449.2:g.42831_42843dup
                      11.

                      rs1491277565 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->CAA [Show Flanks]
                        Chromosome:
                        10:121552024 (GRCh38)
                        10:123311539 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:121552024:AA:AACAA
                        Gene:
                        FGFR2 (Varview)
                        Functional Consequence:
                        genic_upstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        AACAA=0.00017/2 (ALFA)
                        AAC=0.00007/1 (TOMMO)
                        HGVS:
                        12.

                        rs1491225214 has merged into rs35537265 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          AAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                          Chromosome:
                          10:121497137 (GRCh38)
                          10:123256651 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121497130:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                          Gene:
                          FGFR2 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          AAAAAA=0./0 (ALFA)
                          HGVS:
                          NC_000010.11:g.121497137_121497149del, NC_000010.11:g.121497139_121497149del, NC_000010.11:g.121497140_121497149del, NC_000010.11:g.121497141_121497149del, NC_000010.11:g.121497142_121497149del, NC_000010.11:g.121497143_121497149del, NC_000010.11:g.121497144_121497149del, NC_000010.11:g.121497145_121497149del, NC_000010.11:g.121497146_121497149del, NC_000010.11:g.121497147_121497149del, NC_000010.11:g.121497148_121497149del, NC_000010.11:g.121497149del, NC_000010.11:g.121497149dup, NC_000010.11:g.121497148_121497149dup, NC_000010.11:g.121497147_121497149dup, NC_000010.11:g.121497146_121497149dup, NC_000010.11:g.121497145_121497149dup, NC_000010.11:g.121497144_121497149dup, NC_000010.11:g.121497131_121497149dup, NC_000010.10:g.123256651_123256663del, NC_000010.10:g.123256653_123256663del, NC_000010.10:g.123256654_123256663del, NC_000010.10:g.123256655_123256663del, NC_000010.10:g.123256656_123256663del, NC_000010.10:g.123256657_123256663del, NC_000010.10:g.123256658_123256663del, NC_000010.10:g.123256659_123256663del, NC_000010.10:g.123256660_123256663del, NC_000010.10:g.123256661_123256663del, NC_000010.10:g.123256662_123256663del, NC_000010.10:g.123256663del, NC_000010.10:g.123256663dup, NC_000010.10:g.123256662_123256663dup, NC_000010.10:g.123256661_123256663dup, NC_000010.10:g.123256660_123256663dup, NC_000010.10:g.123256659_123256663dup, NC_000010.10:g.123256658_123256663dup, NC_000010.10:g.123256645_123256663dup, NG_012449.2:g.106316_106328del, NG_012449.2:g.106318_106328del, NG_012449.2:g.106319_106328del, NG_012449.2:g.106320_106328del, NG_012449.2:g.106321_106328del, NG_012449.2:g.106322_106328del, NG_012449.2:g.106323_106328del, NG_012449.2:g.106324_106328del, NG_012449.2:g.106325_106328del, NG_012449.2:g.106326_106328del, NG_012449.2:g.106327_106328del, NG_012449.2:g.106328del, NG_012449.2:g.106328dup, NG_012449.2:g.106327_106328dup, NG_012449.2:g.106326_106328dup, NG_012449.2:g.106325_106328dup, NG_012449.2:g.106324_106328dup, NG_012449.2:g.106323_106328dup, NG_012449.2:g.106310_106328dup
                          13.

                          rs1491222146 [Homo sapiens]
                            Variant type:
                            INS
                            Alleles:
                            ->G [Show Flanks]
                            Chromosome:
                            10:121497131 (GRCh38)
                            10:123256646 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:121497131::G
                            Gene:
                            FGFR2 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            G=0./0 (ALFA)
                            HGVS:
                            14.

                            rs1491202703 [Homo sapiens]
                              Variant type:
                              INS
                              Alleles:
                              ->TTCTT [Show Flanks]
                              Chromosome:
                              10:121480123 (GRCh38)
                              10:123239638 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:121480123::TTCTT
                              Gene:
                              FGFR2 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,intron_variant
                              HGVS:
                              15.

                              rs1491159064 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                AA>- [Show Flanks]
                                Chromosome:
                                10:121527591 (GRCh38)
                                10:123287105 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:121527590:AA:
                                Gene:
                                FGFR2 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa
                                MAF:
                                -=0./0 (ALFA)
                                -=0.000014/2 (GnomAD)
                                HGVS:
                                16.

                                rs1491130851 has merged into rs1169688456 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  GAGAGAGAGAGAGA>-,GA,GAGA,GAGAGA,GAGAGAGA,GAGAGAGAGA,GAGAGAGAGAGA,GAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,GAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA [Show Flanks]
                                  Chromosome:
                                  10:121577194 (GRCh38)
                                  10:123336708 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA,NC_000010.11:121577178:AGAGAGAGAGAGAGAGAGAGAGAGAGAGA:AGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGA
                                  Gene:
                                  FGFR2 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_upstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  AGAGAGAGAGAGAGAGA=0./0 (ALFA)
                                  HGVS:
                                  NC_000010.11:g.121577180GA[7], NC_000010.11:g.121577180GA[8], NC_000010.11:g.121577180GA[9], NC_000010.11:g.121577180GA[10], NC_000010.11:g.121577180GA[11], NC_000010.11:g.121577180GA[12], NC_000010.11:g.121577180GA[13], NC_000010.11:g.121577180GA[15], NC_000010.11:g.121577180GA[16], NC_000010.11:g.121577180GA[17], NC_000010.11:g.121577180GA[18], NC_000010.11:g.121577180GA[19], NC_000010.11:g.121577180GA[20], NC_000010.11:g.121577180GA[21], NC_000010.11:g.121577180GA[22], NC_000010.11:g.121577180GA[23], NC_000010.11:g.121577180GA[24], NC_000010.11:g.121577180GA[25], NC_000010.11:g.121577180GA[26], NC_000010.11:g.121577180GA[27], NC_000010.11:g.121577180GA[28], NC_000010.11:g.121577180GA[29], NC_000010.11:g.121577180GA[30], NC_000010.10:g.123336694GA[7], NC_000010.10:g.123336694GA[8], NC_000010.10:g.123336694GA[9], NC_000010.10:g.123336694GA[10], NC_000010.10:g.123336694GA[11], NC_000010.10:g.123336694GA[12], NC_000010.10:g.123336694GA[13], NC_000010.10:g.123336694GA[15], NC_000010.10:g.123336694GA[16], NC_000010.10:g.123336694GA[17], NC_000010.10:g.123336694GA[18], NC_000010.10:g.123336694GA[19], NC_000010.10:g.123336694GA[20], NC_000010.10:g.123336694GA[21], NC_000010.10:g.123336694GA[22], NC_000010.10:g.123336694GA[23], NC_000010.10:g.123336694GA[24], NC_000010.10:g.123336694GA[25], NC_000010.10:g.123336694GA[26], NC_000010.10:g.123336694GA[27], NC_000010.10:g.123336694GA[28], NC_000010.10:g.123336694GA[29], NC_000010.10:g.123336694GA[30], NG_012449.2:g.26253CT[7], NG_012449.2:g.26253CT[8], NG_012449.2:g.26253CT[9], NG_012449.2:g.26253CT[10], NG_012449.2:g.26253CT[11], NG_012449.2:g.26253CT[12], NG_012449.2:g.26253CT[13], NG_012449.2:g.26253CT[15], NG_012449.2:g.26253CT[16], NG_012449.2:g.26253CT[17], NG_012449.2:g.26253CT[18], NG_012449.2:g.26253CT[19], NG_012449.2:g.26253CT[20], NG_012449.2:g.26253CT[21], NG_012449.2:g.26253CT[22], NG_012449.2:g.26253CT[23], NG_012449.2:g.26253CT[24], NG_012449.2:g.26253CT[25], NG_012449.2:g.26253CT[26], NG_012449.2:g.26253CT[27], NG_012449.2:g.26253CT[28], NG_012449.2:g.26253CT[29], NG_012449.2:g.26253CT[30]
                                  17.

                                  rs1491124694 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ->TACACA [Show Flanks]
                                    Chromosome:
                                    10:121524101 (GRCh38)
                                    10:123283616 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:121524101:ACA:ACATACACA
                                    Gene:
                                    FGFR2 (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    ACATACACA=0./0 (ALFA)
                                    ACATAC=0.00005/4 (GnomAD)
                                    HGVS:
                                    18.

                                    rs1491094097 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      CA>- [Show Flanks]
                                      Chromosome:
                                      10:121565176 (GRCh38)
                                      10:123324690 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:121565174:ACA:A
                                      Gene:
                                      FGFR2 (Varview)
                                      Functional Consequence:
                                      genic_upstream_transcript_variant,intron_variant
                                      Validated:
                                      by frequency,by cluster
                                      MAF:
                                      -=0.0054/20 (TWINSUK)
                                      -=0.0062/24 (ALSPAC)
                                      HGVS:
                                      19.

                                      rs1491092946 [Homo sapiens]
                                        Variant type:
                                        INS
                                        Alleles:
                                        ->T [Show Flanks]
                                        Chromosome:
                                        10:121527591 (GRCh38)
                                        10:123287106 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:121527591::T
                                        Gene:
                                        FGFR2 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.00057/5 (GnomAD)
                                        HGVS:
                                        20.

                                        rs1491083741 has merged into rs10678814 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          AAAAAAAAAA>-,AA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                                          Chromosome:
                                          10:121506367 (GRCh38)
                                          10:123265881 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:121506357:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                                          Gene:
                                          FGFR2 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          AAAAAAAAAAA=0./0 (ALFA)
                                          HGVS:
                                          NC_000010.11:g.121506367_121506376del, NC_000010.11:g.121506369_121506376del, NC_000010.11:g.121506372_121506376del, NC_000010.11:g.121506373_121506376del, NC_000010.11:g.121506374_121506376del, NC_000010.11:g.121506375_121506376del, NC_000010.11:g.121506376del, NC_000010.11:g.121506376dup, NC_000010.11:g.121506375_121506376dup, NC_000010.11:g.121506374_121506376dup, NC_000010.11:g.121506373_121506376dup, NC_000010.11:g.121506372_121506376dup, NC_000010.11:g.121506371_121506376dup, NC_000010.11:g.121506370_121506376dup, NC_000010.11:g.121506369_121506376dup, NC_000010.11:g.121506367_121506376dup, NC_000010.11:g.121506366_121506376dup, NC_000010.11:g.121506365_121506376dup, NC_000010.11:g.121506364_121506376dup, NC_000010.11:g.121506363_121506376dup, NC_000010.11:g.121506362_121506376dup, NC_000010.11:g.121506361_121506376dup, NC_000010.11:g.121506360_121506376dup, NC_000010.11:g.121506359_121506376dup, NC_000010.11:g.121506376_121506377insAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.123265881_123265890del, NC_000010.10:g.123265883_123265890del, NC_000010.10:g.123265886_123265890del, NC_000010.10:g.123265887_123265890del, NC_000010.10:g.123265888_123265890del, NC_000010.10:g.123265889_123265890del, NC_000010.10:g.123265890del, NC_000010.10:g.123265890dup, NC_000010.10:g.123265889_123265890dup, NC_000010.10:g.123265888_123265890dup, NC_000010.10:g.123265887_123265890dup, NC_000010.10:g.123265886_123265890dup, NC_000010.10:g.123265885_123265890dup, NC_000010.10:g.123265884_123265890dup, NC_000010.10:g.123265883_123265890dup, NC_000010.10:g.123265881_123265890dup, NC_000010.10:g.123265880_123265890dup, NC_000010.10:g.123265879_123265890dup, NC_000010.10:g.123265878_123265890dup, NC_000010.10:g.123265877_123265890dup, NC_000010.10:g.123265876_123265890dup, NC_000010.10:g.123265875_123265890dup, NC_000010.10:g.123265874_123265890dup, NC_000010.10:g.123265873_123265890dup, NC_000010.10:g.123265890_123265891insAAAAAAAAAAAAAAAAAAAAAA, NG_012449.2:g.97092_97101del, NG_012449.2:g.97094_97101del, NG_012449.2:g.97097_97101del, NG_012449.2:g.97098_97101del, NG_012449.2:g.97099_97101del, NG_012449.2:g.97100_97101del, NG_012449.2:g.97101del, NG_012449.2:g.97101dup, NG_012449.2:g.97100_97101dup, NG_012449.2:g.97099_97101dup, NG_012449.2:g.97098_97101dup, NG_012449.2:g.97097_97101dup, NG_012449.2:g.97096_97101dup, NG_012449.2:g.97095_97101dup, NG_012449.2:g.97094_97101dup, NG_012449.2:g.97092_97101dup, NG_012449.2:g.97091_97101dup, NG_012449.2:g.97090_97101dup, NG_012449.2:g.97089_97101dup, NG_012449.2:g.97088_97101dup, NG_012449.2:g.97087_97101dup, NG_012449.2:g.97086_97101dup, NG_012449.2:g.97085_97101dup, NG_012449.2:g.97084_97101dup, NG_012449.2:g.97101_97102insTTTTTTTTTTTTTTTTTTTTTT

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