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Items: 1 to 20 of 16841

1.

rs1491586218 [Homo sapiens]
    Variant type:
    SNV:
    Alleles:
    TC>-
    Chromosome:
    no mapping
    Canonical SPDI:

    2.

    rs1491559269 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      AA>- [Show Flanks]
      Chromosome:
      19:48107466 (GRCh38)
      19:48610723 (GRCh37)
      Canonical SPDI:
      NC_000019.10:48107465:AA:
      Gene:
      PLA2G4C (Varview)
      Functional Consequence:
      intron_variant,genic_upstream_transcript_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      -=0./0 (ALFA)
      -=0.000015/4 (TOPMED)
      -=0.000022/3 (GnomAD)
      HGVS:

      3.

      rs1491527624 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->A [Show Flanks]
        Chromosome:
        19:48105863 (GRCh38)
        19:48609121 (GRCh37)
        Canonical SPDI:
        NC_000019.10:48105863::A
        Gene:
        PLA2G4C (Varview)
        Functional Consequence:
        intron_variant,genic_upstream_transcript_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        A=0.00025/3 (ALFA)
        A=0.00026/3 (TOMMO)
        A=0.00818/467 (GnomAD)
        HGVS:

        4.

        rs1491520991 has merged into rs544287174 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          TTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
          Chromosome:
          19:48101136 (GRCh38)
          19:48604393 (GRCh37)
          Canonical SPDI:
          NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48101126:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
          Gene:
          PLA2G4C (Varview)
          Functional Consequence:
          genic_upstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          TTTTTTTTTT=0./0 (ALFA)
          T=0.3642/1824 (1000Genomes)
          HGVS:
          NC_000019.10:g.48101136_48101143del, NC_000019.10:g.48101137_48101143del, NC_000019.10:g.48101138_48101143del, NC_000019.10:g.48101139_48101143del, NC_000019.10:g.48101140_48101143del, NC_000019.10:g.48101141_48101143del, NC_000019.10:g.48101142_48101143del, NC_000019.10:g.48101143del, NC_000019.10:g.48101143dup, NC_000019.10:g.48101142_48101143dup, NC_000019.10:g.48101141_48101143dup, NC_000019.10:g.48101140_48101143dup, NC_000019.10:g.48101139_48101143dup, NC_000019.10:g.48101138_48101143dup, NC_000019.10:g.48101137_48101143dup, NC_000019.10:g.48101136_48101143dup, NC_000019.9:g.48604393_48604400del, NC_000019.9:g.48604394_48604400del, NC_000019.9:g.48604395_48604400del, NC_000019.9:g.48604396_48604400del, NC_000019.9:g.48604397_48604400del, NC_000019.9:g.48604398_48604400del, NC_000019.9:g.48604399_48604400del, NC_000019.9:g.48604400del, NC_000019.9:g.48604400dup, NC_000019.9:g.48604399_48604400dup, NC_000019.9:g.48604398_48604400dup, NC_000019.9:g.48604397_48604400dup, NC_000019.9:g.48604396_48604400dup, NC_000019.9:g.48604395_48604400dup, NC_000019.9:g.48604394_48604400dup, NC_000019.9:g.48604393_48604400dup, NG_016021.1:g.14719_14726del, NG_016021.1:g.14720_14726del, NG_016021.1:g.14721_14726del, NG_016021.1:g.14722_14726del, NG_016021.1:g.14723_14726del, NG_016021.1:g.14724_14726del, NG_016021.1:g.14725_14726del, NG_016021.1:g.14726del, NG_016021.1:g.14726dup, NG_016021.1:g.14725_14726dup, NG_016021.1:g.14724_14726dup, NG_016021.1:g.14723_14726dup, NG_016021.1:g.14722_14726dup, NG_016021.1:g.14721_14726dup, NG_016021.1:g.14720_14726dup, NG_016021.1:g.14719_14726dup

          5.

          rs1491510332 has merged into rs1181588598 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            TTTTTTTTTTTTTTTTTTT>-,TTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
            Chromosome:
            19:48046984 (GRCh38)
            19:48550241 (GRCh37)
            Canonical SPDI:
            NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046974:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            TTTTTTTTT=0./0 (ALFA)
            TTTTTTT=0.0008/1 (Korea1K)
            TTTTTTTTTTTTT=0.00826/4 (NorthernSweden)
            HGVS:
            NC_000019.10:g.48046984_48047002del, NC_000019.10:g.48046987_48047002del, NC_000019.10:g.48046989_48047002del, NC_000019.10:g.48046990_48047002del, NC_000019.10:g.48046992_48047002del, NC_000019.10:g.48046993_48047002del, NC_000019.10:g.48046994_48047002del, NC_000019.10:g.48046995_48047002del, NC_000019.10:g.48046996_48047002del, NC_000019.10:g.48046997_48047002del, NC_000019.10:g.48046999_48047002del, NC_000019.10:g.48047000_48047002del, NC_000019.10:g.48047001_48047002del, NC_000019.10:g.48047002del, NC_000019.10:g.48047002dup, NC_000019.10:g.48047001_48047002dup, NC_000019.10:g.48047000_48047002dup, NC_000019.10:g.48046999_48047002dup, NC_000019.10:g.48046998_48047002dup, NC_000019.10:g.48046997_48047002dup, NC_000019.10:g.48046996_48047002dup, NC_000019.10:g.48046995_48047002dup, NC_000019.10:g.48046994_48047002dup, NC_000019.10:g.48046993_48047002dup, NC_000019.10:g.48046992_48047002dup, NC_000019.10:g.48046991_48047002dup, NC_000019.10:g.48046990_48047002dup, NC_000019.9:g.48550241_48550259del, NC_000019.9:g.48550244_48550259del, NC_000019.9:g.48550246_48550259del, NC_000019.9:g.48550247_48550259del, NC_000019.9:g.48550249_48550259del, NC_000019.9:g.48550250_48550259del, NC_000019.9:g.48550251_48550259del, NC_000019.9:g.48550252_48550259del, NC_000019.9:g.48550253_48550259del, NC_000019.9:g.48550254_48550259del, NC_000019.9:g.48550256_48550259del, NC_000019.9:g.48550257_48550259del, NC_000019.9:g.48550258_48550259del, NC_000019.9:g.48550259del, NC_000019.9:g.48550259dup, NC_000019.9:g.48550258_48550259dup, NC_000019.9:g.48550257_48550259dup, NC_000019.9:g.48550256_48550259dup, NC_000019.9:g.48550255_48550259dup, NC_000019.9:g.48550254_48550259dup, NC_000019.9:g.48550253_48550259dup, NC_000019.9:g.48550252_48550259dup, NC_000019.9:g.48550251_48550259dup, NC_000019.9:g.48550250_48550259dup, NC_000019.9:g.48550249_48550259dup, NC_000019.9:g.48550248_48550259dup, NC_000019.9:g.48550247_48550259dup, NG_016021.1:g.68860_68878del, NG_016021.1:g.68863_68878del, NG_016021.1:g.68865_68878del, NG_016021.1:g.68866_68878del, NG_016021.1:g.68868_68878del, NG_016021.1:g.68869_68878del, NG_016021.1:g.68870_68878del, NG_016021.1:g.68871_68878del, NG_016021.1:g.68872_68878del, NG_016021.1:g.68873_68878del, NG_016021.1:g.68875_68878del, NG_016021.1:g.68876_68878del, NG_016021.1:g.68877_68878del, NG_016021.1:g.68878del, NG_016021.1:g.68878dup, NG_016021.1:g.68877_68878dup, NG_016021.1:g.68876_68878dup, NG_016021.1:g.68875_68878dup, NG_016021.1:g.68874_68878dup, NG_016021.1:g.68873_68878dup, NG_016021.1:g.68872_68878dup, NG_016021.1:g.68871_68878dup, NG_016021.1:g.68870_68878dup, NG_016021.1:g.68869_68878dup, NG_016021.1:g.68868_68878dup, NG_016021.1:g.68867_68878dup, NG_016021.1:g.68866_68878dup

            6.

            rs1491505410 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              TC>-
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1491493741 has merged into rs71181636 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                AGAGAGAGAG>-,AGAGAGAG,AGAGAGAGAGAG,AGAGAGAGAGAGAG,AGAGAGAGAGAGAGAG [Show Flanks]
                Chromosome:
                19:48051574 (GRCh38)
                19:48554831 (GRCh37)
                Canonical SPDI:
                NC_000019.10:48051570:GAGAGAGAGAGAG:GAG,NC_000019.10:48051570:GAGAGAGAGAGAG:GAGAGAGAGAG,NC_000019.10:48051570:GAGAGAGAGAGAG:GAGAGAGAGAGAGAG,NC_000019.10:48051570:GAGAGAGAGAGAG:GAGAGAGAGAGAGAGAG,NC_000019.10:48051570:GAGAGAGAGAGAG:GAGAGAGAGAGAGAGAGAG
                Gene:
                PLA2G4C (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                GAGAGAGAGAG=0./0 (ALFA)
                -=0.125/5 (GENOME_DK)
                -=0.1417/85 (NorthernSweden)
                HGVS:

                8.

                rs1491479456 has merged into rs71181639 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AAAAAAAAAAA>-,A,AAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
                  Chromosome:
                  19:48068315 (GRCh38)
                  19:48571572 (GRCh37)
                  Canonical SPDI:
                  NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:48068303:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
                  Gene:
                  PLA2G4C (Varview)
                  Functional Consequence:
                  genic_downstream_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  AAAAAAAAAAAA=0./0 (ALFA)
                  HGVS:
                  NC_000019.10:g.48068315_48068325del, NC_000019.10:g.48068316_48068325del, NC_000019.10:g.48068319_48068325del, NC_000019.10:g.48068322_48068325del, NC_000019.10:g.48068323_48068325del, NC_000019.10:g.48068324_48068325del, NC_000019.10:g.48068325del, NC_000019.10:g.48068325dup, NC_000019.10:g.48068324_48068325dup, NC_000019.10:g.48068323_48068325dup, NC_000019.10:g.48068322_48068325dup, NC_000019.9:g.48571572_48571582del, NC_000019.9:g.48571573_48571582del, NC_000019.9:g.48571576_48571582del, NC_000019.9:g.48571579_48571582del, NC_000019.9:g.48571580_48571582del, NC_000019.9:g.48571581_48571582del, NC_000019.9:g.48571582del, NC_000019.9:g.48571582dup, NC_000019.9:g.48571581_48571582dup, NC_000019.9:g.48571580_48571582dup, NC_000019.9:g.48571579_48571582dup, NG_016021.1:g.47539_47549del, NG_016021.1:g.47540_47549del, NG_016021.1:g.47543_47549del, NG_016021.1:g.47546_47549del, NG_016021.1:g.47547_47549del, NG_016021.1:g.47548_47549del, NG_016021.1:g.47549del, NG_016021.1:g.47549dup, NG_016021.1:g.47548_47549dup, NG_016021.1:g.47547_47549dup, NG_016021.1:g.47546_47549dup

                  9.

                  rs1491469829 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    ->CGTGTGTGTGTGTGTG [Show Flanks]
                    Chromosome:
                    19:48084041 (GRCh38)
                    19:48587299 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:48084041:GTGTGTGTGTGTGTG:GTGTGTGTGTGTGTGCGTGTGTGTGTGTGTG
                    Gene:
                    PLA2G4C (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    GTGTGTGTGTGTGTGCGTGTGTGTGTGTGTG=0.00008/1 (ALFA)
                    GTGTGTGTGTGTGTGC=0.00011/1 (GnomAD)
                    HGVS:

                    10.

                    rs1491453108 [Homo sapiens]
                      Variant type:
                      DEL
                      Alleles:
                      CA>- [Show Flanks]
                      Chromosome:
                      19:48046569 (GRCh38)
                      19:48549826 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:48046568:CA:
                      Validated:
                      by frequency,by alfa
                      MAF:
                      -=0.00008/1 (ALFA)
                      -=0.00029/8 (TOMMO)
                      HGVS:

                      11.

                      rs1491446504 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->CT [Show Flanks]
                        Chromosome:
                        19:48057484 (GRCh38)
                        19:48560742 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:48057484:T:TCT
                        Gene:
                        PLA2G4C (Varview)
                        Functional Consequence:
                        genic_downstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        TCT=0./0 (ALFA)
                        HGVS:

                        12.

                        rs1491444975 [Homo sapiens]
                          Variant type:
                          INS
                          Alleles:
                          ->T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                          Chromosome:
                          19:48046973 (GRCh38)
                          19:48550231 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:48046973::T,NC_000019.10:48046973::TT,NC_000019.10:48046973::TTT,NC_000019.10:48046973::TTTT,NC_000019.10:48046973::TTTTT,NC_000019.10:48046973::TTTTTT,NC_000019.10:48046973::TTTTTTT,NC_000019.10:48046973::TTTTTTTT,NC_000019.10:48046973::TTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48046973::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          TT=0./0 (ALFA)
                          HGVS:
                          NC_000019.10:g.48046973_48046974insT, NC_000019.10:g.48046973_48046974insTT, NC_000019.10:g.48046973_48046974insTTT, NC_000019.10:g.48046973_48046974insTTTT, NC_000019.10:g.48046973_48046974insTTTTT, NC_000019.10:g.48046973_48046974insTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48046973_48046974insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insT, NC_000019.9:g.48550230_48550231insTT, NC_000019.9:g.48550230_48550231insTTT, NC_000019.9:g.48550230_48550231insTTTT, NC_000019.9:g.48550230_48550231insTTTTT, NC_000019.9:g.48550230_48550231insTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48550230_48550231insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016021.1:g.68879_68880insA, NG_016021.1:g.68879_68880insAA, NG_016021.1:g.68879_68880insAAA, NG_016021.1:g.68879_68880insAAAA, NG_016021.1:g.68879_68880insAAAAA, NG_016021.1:g.68879_68880insAAAAAA, NG_016021.1:g.68879_68880insAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.68879_68880insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

                          13.

                          rs1491384247 [Homo sapiens]
                            Variant type:
                            DEL
                            Alleles:
                            CA>- [Show Flanks]
                            Chromosome:
                            19:48068303 (GRCh38)
                            19:48571560 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:48068302:CA:
                            Gene:
                            PLA2G4C (Varview)
                            Functional Consequence:
                            genic_downstream_transcript_variant,intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            -=0.01096/130 (ALFA)
                            -=0.00033/14 (GnomAD)
                            -=0.00241/67 (TOMMO)
                            HGVS:

                            14.

                            rs1491370558 [Homo sapiens]
                              Variant type:
                              DELINS
                              Alleles:
                              ->C [Show Flanks]
                              Chromosome:
                              19:48065276 (GRCh38)
                              19:48568534 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:48065276:C:CC
                              Gene:
                              PLA2G4C (Varview), PLA2G4C-AS1 (Varview)
                              Functional Consequence:
                              genic_downstream_transcript_variant,downstream_transcript_variant,intron_variant,500B_downstream_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              CC=0./0 (ALFA)
                              C=0.00004/2 (GnomAD)
                              HGVS:

                              15.

                              rs1491339452 [Homo sapiens]
                                Variant type:
                                DELINS
                                Alleles:
                                TA>- [Show Flanks]
                                Chromosome:
                                19:48091910 (GRCh38)
                                19:48595167 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:48091908:ATA:A
                                Gene:
                                PLA2G4C (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                A=0.00034/4 (ALFA)
                                -=0.00219/149 (GnomAD)
                                -=0.00249/41 (TOMMO)
                                -=0.02018/35 (Korea1K)
                                HGVS:

                                16.

                                rs1491333149 has merged into rs927559836 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  T>-,TT [Show Flanks]
                                  Chromosome:
                                  19:48058010 (GRCh38)
                                  19:48561267 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:48058009:TTTTTTT:TTTTTT,NC_000019.10:48058009:TTTTTTT:TTTTTTTT
                                  Gene:
                                  PLA2G4C (Varview)
                                  Functional Consequence:
                                  genic_downstream_transcript_variant,intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  TTTTTTTT=0./0 (ALFA)
                                  -=0.000156/1 (1000Genomes)
                                  -=0.000196/52 (TOPMED)
                                  HGVS:

                                  17.

                                  rs1491313614 [Homo sapiens]
                                    Variant type:
                                    DEL
                                    Alleles:
                                    AT>- [Show Flanks]
                                    Chromosome:
                                    19:48092068 (GRCh38)
                                    19:48595325 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:48092067:AT:
                                    Gene:
                                    PLA2G4C (Varview)
                                    Functional Consequence:
                                    intron_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    -=0.001042/17 (ALFA)
                                    -=0.001167/137 (GnomAD)
                                    -=0.00203/13 (1000Genomes)
                                    HGVS:

                                    18.

                                    rs1491313107 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      ->ATATATATATATATATATTT,ATATATATATATATATT,ATATATATATATATATTT,ATATATATATATATT,ATATATATATATATTT,ATATATATATATATTTT,ATATATATATATATTTTT,ATATATATATATT,ATATATATATATTT,ATATATATATATTTT,ATATATATATATTTTT,ATATATATATATTTTTT,ATATATATATATTTTTTTT,ATATATATATT,ATATATATATTT,ATATATATATTTT,ATATATATATTTTT,ATATATATATTTTTT,ATATATATATTTTTTT,ATATATATT,ATATATATTT,ATATATATTTT,ATATATATTTTT,ATATATATTTTTT,ATATATATTTTTTT,ATATATT,ATATATTT,ATATATTTT,ATATATTTTT,ATATATTTTTT,ATATATTTTTTT,ATATATTTTTTTT,ATATATTTTTTTTT,ATATT,ATATTT,ATATTTT,ATATTTTT,ATATTTTTT,ATATTTTTTT,ATATTTTTTTT,ATATTTTTTTTT,ATATTTTTTTTTTT,ATT,ATTT,ATTTT,ATTTTT,ATTTTTT,ATTTTTTT,ATTTTTTTT,ATTTTTTTTT,ATTTTTTTTTT,ATTTTTTTTTTT [Show Flanks]
                                      Chromosome:
                                      19:48101126 (GRCh38)
                                      19:48604384 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:48101126:T:TATATATATATATATATATTT,NC_000019.10:48101126:T:TATATATATATATATATT,NC_000019.10:48101126:T:TATATATATATATATATTT,NC_000019.10:48101126:T:TATATATATATATATT,NC_000019.10:48101126:T:TATATATATATATATTT,NC_000019.10:48101126:T:TATATATATATATATTTT,NC_000019.10:48101126:T:TATATATATATATATTTTT,NC_000019.10:48101126:T:TATATATATATATT,NC_000019.10:48101126:T:TATATATATATATTT,NC_000019.10:48101126:T:TATATATATATATTTT,NC_000019.10:48101126:T:TATATATATATATTTTT,NC_000019.10:48101126:T:TATATATATATATTTTTT,NC_000019.10:48101126:T:TATATATATATATTTTTTTT,NC_000019.10:48101126:T:TATATATATATT,NC_000019.10:48101126:T:TATATATATATTT,NC_000019.10:48101126:T:TATATATATATTTT,NC_000019.10:48101126:T:TATATATATATTTTT,NC_000019.10:48101126:T:TATATATATATTTTTT,NC_000019.10:48101126:T:TATATATATATTTTTTT,NC_000019.10:48101126:T:TATATATATT,NC_000019.10:48101126:T:TATATATATTT,NC_000019.10:48101126:T:TATATATATTTT,NC_000019.10:48101126:T:TATATATATTTTT,NC_000019.10:48101126:T:TATATATATTTTTT,NC_000019.10:48101126:T:TATATATATTTTTTT,NC_000019.10:48101126:T:TATATATT,NC_000019.10:48101126:T:TATATATTT,NC_000019.10:48101126:T:TATATATTTT,NC_000019.10:48101126:T:TATATATTTTT,NC_000019.10:48101126:T:TATATATTTTTT,NC_000019.10:48101126:T:TATATATTTTTTT,NC_000019.10:48101126:T:TATATATTTTTTTT,NC_000019.10:48101126:T:TATATATTTTTTTTT,NC_000019.10:48101126:T:TATATT,NC_000019.10:48101126:T:TATATTT,NC_000019.10:48101126:T:TATATTTT,NC_000019.10:48101126:T:TATATTTTT,NC_000019.10:48101126:T:TATATTTTTT,NC_000019.10:48101126:T:TATATTTTTTT,NC_000019.10:48101126:T:TATATTTTTTTT,NC_000019.10:48101126:T:TATATTTTTTTTT,NC_000019.10:48101126:T:TATATTTTTTTTTTT,NC_000019.10:48101126:T:TATT,NC_000019.10:48101126:T:TATTT,NC_000019.10:48101126:T:TATTTT,NC_000019.10:48101126:T:TATTTTT,NC_000019.10:48101126:T:TATTTTTT,NC_000019.10:48101126:T:TATTTTTTT,NC_000019.10:48101126:T:TATTTTTTTT,NC_000019.10:48101126:T:TATTTTTTTTT,NC_000019.10:48101126:T:TATTTTTTTTTT,NC_000019.10:48101126:T:TATTTTTTTTTTT
                                      Gene:
                                      PLA2G4C (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_upstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TATATATATATATATT=0./0 (ALFA)
                                      TATATATATATTTTT=0.000004/1 (TOPMED)
                                      HGVS:
                                      NC_000019.10:g.48101127TA[9]TTT[1], NC_000019.10:g.48101127TA[8]TT[1], NC_000019.10:g.48101127TA[8]TTT[1], NC_000019.10:g.48101127TA[7]TT[1], NC_000019.10:g.48101127TA[7]TTT[1], NC_000019.10:g.48101127TA[7]T[4], NC_000019.10:g.48101127TA[7]T[5], NC_000019.10:g.48101127TA[6]TT[1], NC_000019.10:g.48101127TA[6]TTT[1], NC_000019.10:g.48101127TA[6]T[4], NC_000019.10:g.48101127TA[6]T[5], NC_000019.10:g.48101127TA[6]T[6], NC_000019.10:g.48101127TA[6]T[8], NC_000019.10:g.48101127TA[5]TT[1], NC_000019.10:g.48101127TA[5]TTT[1], NC_000019.10:g.48101127TA[5]T[4], NC_000019.10:g.48101127TA[5]T[5], NC_000019.10:g.48101127TA[5]T[6], NC_000019.10:g.48101127TA[5]T[7], NC_000019.10:g.48101127TA[4]TT[1], NC_000019.10:g.48101127TA[4]TTT[1], NC_000019.10:g.48101127TA[4]T[4], NC_000019.10:g.48101127TA[4]T[5], NC_000019.10:g.48101127TA[4]T[6], NC_000019.10:g.48101127TA[4]T[7], NC_000019.10:g.48101127TA[3]TT[1], NC_000019.10:g.48101127TA[3]TTT[1], NC_000019.10:g.48101127TA[3]T[4], NC_000019.10:g.48101127TA[3]T[5], NC_000019.10:g.48101127TA[3]T[6], NC_000019.10:g.48101127TA[3]T[7], NC_000019.10:g.48101127TA[3]T[8], NC_000019.10:g.48101127TA[3]T[9], NC_000019.10:g.48101127TA[2]TT[1], NC_000019.10:g.48101127TA[2]TTT[1], NC_000019.10:g.48101127TA[2]T[4], NC_000019.10:g.48101127TA[2]T[5], NC_000019.10:g.48101127TA[2]T[6], NC_000019.10:g.48101127TA[2]T[7], NC_000019.10:g.48101127TA[2]T[8], NC_000019.10:g.48101127TA[2]T[9], NC_000019.10:g.48101127TA[2]T[11], NC_000019.10:g.48101127_48101128insATT, NC_000019.10:g.48101127_48101128insATTT, NC_000019.10:g.48101127_48101128insATTTT, NC_000019.10:g.48101127_48101128insATTTTT, NC_000019.10:g.48101127_48101128insATTTTTT, NC_000019.10:g.48101127_48101128insATTTTTTT, NC_000019.10:g.48101127_48101128insATTTTTTTT, NC_000019.10:g.48101127_48101128insATTTTTTTTT, NC_000019.10:g.48101127_48101128insATTTTTTTTTT, NC_000019.10:g.48101127_48101128insATTTTTTTTTTT, NC_000019.9:g.48604384TA[9]TTT[1], NC_000019.9:g.48604384TA[8]TT[1], NC_000019.9:g.48604384TA[8]TTT[1], NC_000019.9:g.48604384TA[7]TT[1], NC_000019.9:g.48604384TA[7]TTT[1], NC_000019.9:g.48604384TA[7]T[4], NC_000019.9:g.48604384TA[7]T[5], NC_000019.9:g.48604384TA[6]TT[1], NC_000019.9:g.48604384TA[6]TTT[1], NC_000019.9:g.48604384TA[6]T[4], NC_000019.9:g.48604384TA[6]T[5], NC_000019.9:g.48604384TA[6]T[6], NC_000019.9:g.48604384TA[6]T[8], NC_000019.9:g.48604384TA[5]TT[1], NC_000019.9:g.48604384TA[5]TTT[1], NC_000019.9:g.48604384TA[5]T[4], NC_000019.9:g.48604384TA[5]T[5], NC_000019.9:g.48604384TA[5]T[6], NC_000019.9:g.48604384TA[5]T[7], NC_000019.9:g.48604384TA[4]TT[1], NC_000019.9:g.48604384TA[4]TTT[1], NC_000019.9:g.48604384TA[4]T[4], NC_000019.9:g.48604384TA[4]T[5], NC_000019.9:g.48604384TA[4]T[6], NC_000019.9:g.48604384TA[4]T[7], NC_000019.9:g.48604384TA[3]TT[1], NC_000019.9:g.48604384TA[3]TTT[1], NC_000019.9:g.48604384TA[3]T[4], NC_000019.9:g.48604384TA[3]T[5], NC_000019.9:g.48604384TA[3]T[6], NC_000019.9:g.48604384TA[3]T[7], NC_000019.9:g.48604384TA[3]T[8], NC_000019.9:g.48604384TA[3]T[9], NC_000019.9:g.48604384TA[2]TT[1], NC_000019.9:g.48604384TA[2]TTT[1], NC_000019.9:g.48604384TA[2]T[4], NC_000019.9:g.48604384TA[2]T[5], NC_000019.9:g.48604384TA[2]T[6], NC_000019.9:g.48604384TA[2]T[7], NC_000019.9:g.48604384TA[2]T[8], NC_000019.9:g.48604384TA[2]T[9], NC_000019.9:g.48604384TA[2]T[11], NC_000019.9:g.48604384_48604385insATT, NC_000019.9:g.48604384_48604385insATTT, NC_000019.9:g.48604384_48604385insATTTT, NC_000019.9:g.48604384_48604385insATTTTT, NC_000019.9:g.48604384_48604385insATTTTTT, NC_000019.9:g.48604384_48604385insATTTTTTT, NC_000019.9:g.48604384_48604385insATTTTTTTT, NC_000019.9:g.48604384_48604385insATTTTTTTTT, NC_000019.9:g.48604384_48604385insATTTTTTTTTT, NC_000019.9:g.48604384_48604385insATTTTTTTTTTT, NG_016021.1:g.14726_14727insAATATATATATATATATATA, NG_016021.1:g.14726_14727insATATATATATATATATA, NG_016021.1:g.14726_14727insAATATATATATATATATA, NG_016021.1:g.14726_14727insATATATATATATATA, NG_016021.1:g.14726_14727insAATATATATATATATA, NG_016021.1:g.14726A[4]TA[7], NG_016021.1:g.14726A[5]TA[7], NG_016021.1:g.14726_14727insATATATATATATA, NG_016021.1:g.14726_14727insAATATATATATATA, NG_016021.1:g.14726A[4]TA[6], NG_016021.1:g.14726A[5]TA[6], NG_016021.1:g.14726A[6]TA[6], NG_016021.1:g.14726A[8]TA[6], NG_016021.1:g.14726_14727insATATATATATA, NG_016021.1:g.14726_14727insAATATATATATA, NG_016021.1:g.14726A[4]TA[5], NG_016021.1:g.14726A[5]TA[5], NG_016021.1:g.14726A[6]TA[5], NG_016021.1:g.14726A[7]TA[5], NG_016021.1:g.14726_14727insATATATATA, NG_016021.1:g.14726_14727insAATATATATA, NG_016021.1:g.14726A[4]TA[4], NG_016021.1:g.14726A[5]TA[4], NG_016021.1:g.14726A[6]TA[4], NG_016021.1:g.14726A[7]TA[4], NG_016021.1:g.14726_14727insATATATA, NG_016021.1:g.14726_14727insAATATATA, NG_016021.1:g.14726A[4]TA[3], NG_016021.1:g.14726A[5]TA[3], NG_016021.1:g.14726A[6]TA[3], NG_016021.1:g.14726A[7]TA[3], NG_016021.1:g.14726A[8]TA[3], NG_016021.1:g.14726A[9]TA[3], NG_016021.1:g.14726_14727insATATA, NG_016021.1:g.14726_14727insAATATA, NG_016021.1:g.14726A[4]TA[2], NG_016021.1:g.14726A[5]TA[2], NG_016021.1:g.14726A[6]TA[2], NG_016021.1:g.14726A[7]TA[2], NG_016021.1:g.14726A[8]TA[2], NG_016021.1:g.14726A[9]TA[2], NG_016021.1:g.14726A[11]TA[2], NG_016021.1:g.14726_14727insATA, NG_016021.1:g.14726_14727insAATA, NG_016021.1:g.14726A[4]TA[1], NG_016021.1:g.14726A[5]TA[1], NG_016021.1:g.14726A[6]TA[1], NG_016021.1:g.14726A[7]TA[1], NG_016021.1:g.14726A[8]TA[1], NG_016021.1:g.14726A[9]TA[1], NG_016021.1:g.14726A[10]TA[1], NG_016021.1:g.14726A[11]TA[1]

                                      19.

                                      rs1491311677 has merged into rs199744302 [Homo sapiens]
                                        Variant type:
                                        DELINS
                                        Alleles:
                                        AAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA [Show Flanks]
                                        Chromosome:
                                        19:48066098 (GRCh38)
                                        19:48569355 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:48066087:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
                                        Gene:
                                        PLA2G4C (Varview)
                                        Functional Consequence:
                                        intron_variant,genic_downstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        AAAAAAAAAAAAAA=0./0 (ALFA)
                                        -=0.000008/2 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1491293432 has merged into rs1171271257 [Homo sapiens]
                                          Variant type:
                                          DELINS
                                          Alleles:
                                          TTTTTTTTTTTTTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
                                          Chromosome:
                                          19:48057496 (GRCh38)
                                          19:48560753 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:48057483:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
                                          Gene:
                                          PLA2G4C (Varview)
                                          Functional Consequence:
                                          genic_downstream_transcript_variant,intron_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          TTTTTTTTTTTT=0./0 (ALFA)
                                          HGVS:
                                          NC_000019.10:g.48057496_48057509del, NC_000019.10:g.48057497_48057509del, NC_000019.10:g.48057498_48057509del, NC_000019.10:g.48057500_48057509del, NC_000019.10:g.48057501_48057509del, NC_000019.10:g.48057502_48057509del, NC_000019.10:g.48057503_48057509del, NC_000019.10:g.48057504_48057509del, NC_000019.10:g.48057505_48057509del, NC_000019.10:g.48057506_48057509del, NC_000019.10:g.48057507_48057509del, NC_000019.10:g.48057508_48057509del, NC_000019.10:g.48057509del, NC_000019.10:g.48057509dup, NC_000019.10:g.48057508_48057509dup, NC_000019.10:g.48057507_48057509dup, NC_000019.10:g.48057506_48057509dup, NC_000019.10:g.48057505_48057509dup, NC_000019.10:g.48057504_48057509dup, NC_000019.10:g.48057503_48057509dup, NC_000019.10:g.48057502_48057509dup, NC_000019.10:g.48057501_48057509dup, NC_000019.10:g.48057500_48057509dup, NC_000019.10:g.48057499_48057509dup, NC_000019.10:g.48057498_48057509dup, NC_000019.10:g.48057497_48057509dup, NC_000019.10:g.48057496_48057509dup, NC_000019.10:g.48057495_48057509dup, NC_000019.10:g.48057494_48057509dup, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.48057509_48057510insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560753_48560766del, NC_000019.9:g.48560754_48560766del, NC_000019.9:g.48560755_48560766del, NC_000019.9:g.48560757_48560766del, NC_000019.9:g.48560758_48560766del, NC_000019.9:g.48560759_48560766del, NC_000019.9:g.48560760_48560766del, NC_000019.9:g.48560761_48560766del, NC_000019.9:g.48560762_48560766del, NC_000019.9:g.48560763_48560766del, NC_000019.9:g.48560764_48560766del, NC_000019.9:g.48560765_48560766del, NC_000019.9:g.48560766del, NC_000019.9:g.48560766dup, NC_000019.9:g.48560765_48560766dup, NC_000019.9:g.48560764_48560766dup, NC_000019.9:g.48560763_48560766dup, NC_000019.9:g.48560762_48560766dup, NC_000019.9:g.48560761_48560766dup, NC_000019.9:g.48560760_48560766dup, NC_000019.9:g.48560759_48560766dup, NC_000019.9:g.48560758_48560766dup, NC_000019.9:g.48560757_48560766dup, NC_000019.9:g.48560756_48560766dup, NC_000019.9:g.48560755_48560766dup, NC_000019.9:g.48560754_48560766dup, NC_000019.9:g.48560753_48560766dup, NC_000019.9:g.48560752_48560766dup, NC_000019.9:g.48560751_48560766dup, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.48560766_48560767insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_016021.1:g.58356_58369del, NG_016021.1:g.58357_58369del, NG_016021.1:g.58358_58369del, NG_016021.1:g.58360_58369del, NG_016021.1:g.58361_58369del, NG_016021.1:g.58362_58369del, NG_016021.1:g.58363_58369del, NG_016021.1:g.58364_58369del, NG_016021.1:g.58365_58369del, NG_016021.1:g.58366_58369del, NG_016021.1:g.58367_58369del, NG_016021.1:g.58368_58369del, NG_016021.1:g.58369del, NG_016021.1:g.58369dup, NG_016021.1:g.58368_58369dup, NG_016021.1:g.58367_58369dup, NG_016021.1:g.58366_58369dup, NG_016021.1:g.58365_58369dup, NG_016021.1:g.58364_58369dup, NG_016021.1:g.58363_58369dup, NG_016021.1:g.58362_58369dup, NG_016021.1:g.58361_58369dup, NG_016021.1:g.58360_58369dup, NG_016021.1:g.58359_58369dup, NG_016021.1:g.58358_58369dup, NG_016021.1:g.58357_58369dup, NG_016021.1:g.58356_58369dup, NG_016021.1:g.58355_58369dup, NG_016021.1:g.58354_58369dup, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_016021.1:g.58369_58370insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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