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Items: 1 to 20 of 36000

1.

rs1491512762 has merged into rs59902893 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    CACACACACACACACACACACACACACACACACA>-,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACACACA [Show Flanks]
    Chromosome:
    1:71234459 (GRCh38)
    1:71700142 (GRCh37)
    Canonical SPDI:
    NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000001.11:71234437:ACACACACACACACACACACACACACACACACACACACACACACACACACACACA:ACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACA
    Gene:
    ZRANB2-DT (Varview)
    Functional Consequence:
    intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    ACACACACACACACACACACACACACA=0./0 (ALFA)
    HGVS:
    NC_000001.11:g.71234439CA[10], NC_000001.11:g.71234439CA[12], NC_000001.11:g.71234439CA[13], NC_000001.11:g.71234439CA[14], NC_000001.11:g.71234439CA[15], NC_000001.11:g.71234439CA[16], NC_000001.11:g.71234439CA[17], NC_000001.11:g.71234439CA[18], NC_000001.11:g.71234439CA[19], NC_000001.11:g.71234439CA[20], NC_000001.11:g.71234439CA[21], NC_000001.11:g.71234439CA[22], NC_000001.11:g.71234439CA[23], NC_000001.11:g.71234439CA[24], NC_000001.11:g.71234439CA[25], NC_000001.11:g.71234439CA[26], NC_000001.11:g.71234439CA[28], NC_000001.11:g.71234439CA[29], NC_000001.11:g.71234439CA[30], NC_000001.11:g.71234439CA[31], NC_000001.10:g.71700122CA[10], NC_000001.10:g.71700122CA[12], NC_000001.10:g.71700122CA[13], NC_000001.10:g.71700122CA[14], NC_000001.10:g.71700122CA[15], NC_000001.10:g.71700122CA[16], NC_000001.10:g.71700122CA[17], NC_000001.10:g.71700122CA[18], NC_000001.10:g.71700122CA[19], NC_000001.10:g.71700122CA[20], NC_000001.10:g.71700122CA[21], NC_000001.10:g.71700122CA[22], NC_000001.10:g.71700122CA[23], NC_000001.10:g.71700122CA[24], NC_000001.10:g.71700122CA[25], NC_000001.10:g.71700122CA[26], NC_000001.10:g.71700122CA[28], NC_000001.10:g.71700122CA[29], NC_000001.10:g.71700122CA[30], NC_000001.10:g.71700122CA[31]

    2.

    rs1491467303 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      TA>- [Show Flanks]
      Chromosome:
      1:71160918 (GRCh38)
      1:71626601 (GRCh37)
      Canonical SPDI:
      NC_000001.11:71160916:ATA:A
      Gene:
      ZRANB2-DT (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      A=0./0 (ALFA)
      -=0.00003/4 (GnomAD)
      HGVS:

      3.

      rs1491437962 has merged into rs11451861 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        AAAAAAAAAAAAAA>-,A,AAA,AAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
        Chromosome:
        1:71180888 (GRCh38)
        1:71646571 (GRCh37)
        Canonical SPDI:
        NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:71180876:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
        Gene:
        ZRANB2-DT (Varview)
        Functional Consequence:
        intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        AAAAAAAAAAA=0./0 (ALFA)
        -=0.000174/46 (TOPMED)
        HGVS:
        NC_000001.11:g.71180888_71180901del, NC_000001.11:g.71180889_71180901del, NC_000001.11:g.71180891_71180901del, NC_000001.11:g.71180894_71180901del, NC_000001.11:g.71180896_71180901del, NC_000001.11:g.71180898_71180901del, NC_000001.11:g.71180899_71180901del, NC_000001.11:g.71180900_71180901del, NC_000001.11:g.71180901del, NC_000001.11:g.71180901dup, NC_000001.11:g.71180900_71180901dup, NC_000001.11:g.71180899_71180901dup, NC_000001.11:g.71180898_71180901dup, NC_000001.11:g.71180897_71180901dup, NC_000001.11:g.71180896_71180901dup, NC_000001.11:g.71180895_71180901dup, NC_000001.11:g.71180894_71180901dup, NC_000001.11:g.71180893_71180901dup, NC_000001.11:g.71180892_71180901dup, NC_000001.11:g.71180891_71180901dup, NC_000001.11:g.71180889_71180901dup, NC_000001.11:g.71180901_71180902insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.11:g.71180901_71180902insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.71646571_71646584del, NC_000001.10:g.71646572_71646584del, NC_000001.10:g.71646574_71646584del, NC_000001.10:g.71646577_71646584del, NC_000001.10:g.71646579_71646584del, NC_000001.10:g.71646581_71646584del, NC_000001.10:g.71646582_71646584del, NC_000001.10:g.71646583_71646584del, NC_000001.10:g.71646584del, NC_000001.10:g.71646584dup, NC_000001.10:g.71646583_71646584dup, NC_000001.10:g.71646582_71646584dup, NC_000001.10:g.71646581_71646584dup, NC_000001.10:g.71646580_71646584dup, NC_000001.10:g.71646579_71646584dup, NC_000001.10:g.71646578_71646584dup, NC_000001.10:g.71646577_71646584dup, NC_000001.10:g.71646576_71646584dup, NC_000001.10:g.71646575_71646584dup, NC_000001.10:g.71646574_71646584dup, NC_000001.10:g.71646572_71646584dup, NC_000001.10:g.71646584_71646585insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000001.10:g.71646584_71646585insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

        4.

        rs1491384268 has merged into rs11344974 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          TTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT [Show Flanks]
          Chromosome:
          1:71089351 (GRCh38)
          1:71555034 (GRCh37)
          Canonical SPDI:
          NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:71089339:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
          Gene:
          ZRANB2-DT (Varview), LOC105378795 (Varview)
          Functional Consequence:
          upstream_transcript_variant,2KB_upstream_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TTTTTTTTTTTTTT=0./0 (ALFA)
          -=0.000008/2 (TOPMED)
          -=0.078333/47 (NorthernSweden)
          -=0.352236/1764 (1000Genomes)
          HGVS:

          5.

          rs1491351378 has merged into rs199805916 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TA>-,TATA,TATATA [Show Flanks]
            Chromosome:
            1:71092516 (GRCh38)
            1:71558199 (GRCh37)
            Canonical SPDI:
            NC_000001.11:71092513:TATA:TA,NC_000001.11:71092513:TATA:TATATA,NC_000001.11:71092513:TATA:TATATATA
            Gene:
            ZRANB2-DT (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TATATATA=0./0 (ALFA)
            -=0.00201/9 (Estonian)
            -=0.00301/50 (TOMMO)
            -=0.00983/18 (Korea1K)
            HGVS:

            6.

            rs1491308159 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->CA,CACA,CACACA [Show Flanks]
              Chromosome:
              1:71092514 (GRCh38)
              1:71558198 (GRCh37)
              Canonical SPDI:
              NC_000001.11:71092514:A:ACA,NC_000001.11:71092514:A:ACACA,NC_000001.11:71092514:A:ACACACA
              Gene:
              ZRANB2-DT (Varview)
              Functional Consequence:
              intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              ACACA=0./0 (ALFA)
              AC=0.00002/1 (GnomAD)
              ACAC=0.00014/2 (TOMMO)
              HGVS:

              7.

              rs1491294130 [Homo sapiens]
                Variant type:
                DEL
                Alleles:
                AA>- [Show Flanks]
                Chromosome:
                1:71125317 (GRCh38)
                1:71591000 (GRCh37)
                Canonical SPDI:
                NC_000001.11:71125316:AA:
                Gene:
                ZRANB2-DT (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                -=0./0 (ALFA)
                -=0.000464/13 (TOMMO)
                -=0.029191/3859 (GnomAD)
                -=0.033885/217 (1000Genomes)
                HGVS:

                8.

                rs1491243890 [Homo sapiens]
                  Variant type:
                  INS
                  Alleles:
                  ->C [Show Flanks]
                  Chromosome:
                  1:71180877 (GRCh38)
                  1:71646561 (GRCh37)
                  Canonical SPDI:
                  NC_000001.11:71180877::C
                  Gene:
                  ZRANB2-DT (Varview)
                  Functional Consequence:
                  intron_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  C=0./0 (ALFA)
                  HGVS:

                  9.

                  rs1491226213 [Homo sapiens]
                    Variant type:
                    INS
                    Alleles:
                    ->TT [Show Flanks]
                    Chromosome:
                    1:71234438 (GRCh38)
                    1:71700122 (GRCh37)
                    Canonical SPDI:
                    NC_000001.11:71234438::TT
                    Gene:
                    ZRANB2-DT (Varview)
                    Functional Consequence:
                    intron_variant
                    HGVS:

                    10.

                    rs1491225089 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AA>- [Show Flanks]
                      Chromosome:
                      1:71083543 (GRCh38)
                      1:71549226 (GRCh37)
                      Canonical SPDI:
                      NC_000001.11:71083541:AAA:A
                      Gene:
                      ZRANB2-DT (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      -=0.0132/51 (ALSPAC)
                      -=0.0272/101 (TWINSUK)
                      HGVS:

                      11.

                      rs1491214292 [Homo sapiens]
                        Variant type:
                        INS
                        Alleles:
                        ->TGTGTGTGTG,TGTGTGTGTGTG,TGTGTGTGTGTGTG,TGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG [Show Flanks]
                        Chromosome:
                        1:71125317 (GRCh38)
                        1:71591001 (GRCh37)
                        Canonical SPDI:
                        NC_000001.11:71125317::TGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTGTGTGTGTGTGTG,NC_000001.11:71125317::TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
                        Gene:
                        ZRANB2-DT (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        TGTGTGTGTGTGTGTGTG=0./0 (ALFA)
                        HGVS:
                        NC_000001.11:g.71125317_71125318insTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.11:g.71125317_71125318insTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG, NC_000001.10:g.71591000_71591001insTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG

                        12.

                        rs1491212394 [Homo sapiens]
                          Variant type:
                          INS
                          Alleles:
                          ->A [Show Flanks]
                          Chromosome:
                          1:71089340 (GRCh38)
                          1:71555024 (GRCh37)
                          Canonical SPDI:
                          NC_000001.11:71089340::A
                          Gene:
                          ZRANB2-DT (Varview), LOC105378795 (Varview)
                          Functional Consequence:
                          intron_variant,upstream_transcript_variant,2KB_upstream_variant
                          Validated:
                          by frequency
                          MAF:
                          A=0.00002/1 (GnomAD)
                          HGVS:

                          13.

                          rs1491209463 [Homo sapiens]
                            Variant type:
                            INS
                            Alleles:
                            ->G [Show Flanks]
                            Chromosome:
                            1:71114367 (GRCh38)
                            1:71580051 (GRCh37)
                            Canonical SPDI:
                            NC_000001.11:71114367::G
                            Gene:
                            ZRANB2-DT (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            G=0./0 (ALFA)
                            G=0.00012/2 (GnomAD)
                            HGVS:

                            14.

                            rs1491186985 has merged into rs78591404 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              TA>-,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA [Show Flanks]
                              Chromosome:
                              1:71234437 (GRCh38)
                              1:71700120 (GRCh37)
                              Canonical SPDI:
                              NC_000001.11:71234431:ATATATA:ATATA,NC_000001.11:71234431:ATATATA:ATATATATA,NC_000001.11:71234431:ATATATA:ATATATATATA,NC_000001.11:71234431:ATATATA:ATATATATATATA,NC_000001.11:71234431:ATATATA:ATATATATATATATA,NC_000001.11:71234431:ATATATA:ATATATATATATATATA,NC_000001.11:71234431:ATATATA:ATATATATATATATATATA
                              Gene:
                              ZRANB2-DT (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              ATATATATA=0./0 (ALFA)
                              ATAT=0.00309/5 (Korea1K)
                              HGVS:

                              15.

                              rs1491149748 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                ->CT [Show Flanks]
                                Chromosome:
                                1:71234432 (GRCh38)
                                1:71700116 (GRCh37)
                                Canonical SPDI:
                                NC_000001.11:71234432:T:TCT
                                Gene:
                                ZRANB2-DT (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency
                                MAF:
                                TC=0.001/8 (GnomAD)
                                HGVS:

                                16.

                                rs1491089826 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  ->GTATATATATATATATACATATATAT [Show Flanks]
                                  Chromosome:
                                  1:71136177 (GRCh38)
                                  1:71601861 (GRCh37)
                                  Canonical SPDI:
                                  NC_000001.11:71136177:ATATATAT:ATATATATGTATATATATATATATACATATATAT
                                  Gene:
                                  ZRANB2-DT (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  ATATATATGTATATATATATATATACATATATAT=0./0 (ALFA)
                                  ATATATATGTATATATATATATATAC=0.00004/1 (TOMMO)
                                  ATATATATGTATATATATATATATAC=0.00016/3 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1491060493 has merged into rs1041983632 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    TC>-,TCTC [Show Flanks]
                                    Chromosome:
                                    1:71092553 (GRCh38)
                                    1:71558236 (GRCh37)
                                    Canonical SPDI:
                                    NC_000001.11:71092551:CTC:C,NC_000001.11:71092551:CTC:CTCTC
                                    Gene:
                                    ZRANB2-DT (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    CTCTC=0./0 (ALFA)
                                    CT=0.000036/5 (GnomAD)
                                    HGVS:

                                    18.

                                    rs1491037930 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      AG>- [Show Flanks]
                                      Chromosome:
                                      1:71197796 (GRCh38)
                                      1:71663479 (GRCh37)
                                      Canonical SPDI:
                                      NC_000001.11:71197793:AGAG:AG
                                      Gene:
                                      ZRANB2-DT (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      AGAG=0./0 (ALFA)
                                      -=0.000011/3 (TOPMED)
                                      -=0.000177/3 (TOMMO)
                                      HGVS:

                                      19.

                                      rs1491018189 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        ->GTATATATATATATATATATATACATAT [Show Flanks]
                                        Chromosome:
                                        1:71136181 (GRCh38)
                                        1:71601865 (GRCh37)
                                        Canonical SPDI:
                                        NC_000001.11:71136181:ATAT:ATATGTATATATATATATATATATATACATAT
                                        Gene:
                                        ZRANB2-DT (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        HGVS:

                                        20.

                                        rs1490997110 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          T>A [Show Flanks]
                                          Chromosome:
                                          1:71177087 (GRCh38)
                                          1:71642770 (GRCh37)
                                          Canonical SPDI:
                                          NC_000001.11:71177086:T:A
                                          Gene:
                                          ZRANB2-DT (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency,by alfa
                                          MAF:
                                          A=0.000071/1 (ALFA)
                                          A=0.000004/1 (TOPMED)
                                          HGVS:

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