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Items: 1 to 20 of 2962

1.

rs1491589125 has merged into rs60336711 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AAAAAAAAAAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
    Chromosome:
    19:14333241 (GRCh38)
    19:14444053 (GRCh37)
    Canonical SPDI:
    NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14333231:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
    Gene:
    LINC01842 (Varview), LINC01841 (Varview)
    Functional Consequence:
    upstream_transcript_variant,2KB_upstream_variant,intron_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    AAAAAAAAA=0./0 (ALFA)
    HGVS:
    NC_000019.10:g.14333241_14333258del, NC_000019.10:g.14333245_14333258del, NC_000019.10:g.14333246_14333258del, NC_000019.10:g.14333247_14333258del, NC_000019.10:g.14333248_14333258del, NC_000019.10:g.14333249_14333258del, NC_000019.10:g.14333250_14333258del, NC_000019.10:g.14333251_14333258del, NC_000019.10:g.14333252_14333258del, NC_000019.10:g.14333253_14333258del, NC_000019.10:g.14333254_14333258del, NC_000019.10:g.14333255_14333258del, NC_000019.10:g.14333256_14333258del, NC_000019.10:g.14333257_14333258del, NC_000019.10:g.14333258del, NC_000019.10:g.14333258dup, NC_000019.10:g.14333257_14333258dup, NC_000019.10:g.14333256_14333258dup, NC_000019.10:g.14333255_14333258dup, NC_000019.10:g.14333254_14333258dup, NC_000019.10:g.14333253_14333258dup, NC_000019.10:g.14333252_14333258dup, NC_000019.10:g.14333251_14333258dup, NC_000019.10:g.14333250_14333258dup, NC_000019.10:g.14333249_14333258dup, NC_000019.10:g.14333248_14333258dup, NC_000019.10:g.14333247_14333258dup, NC_000019.10:g.14333246_14333258dup, NC_000019.10:g.14333245_14333258dup, NC_000019.10:g.14333244_14333258dup, NC_000019.10:g.14333243_14333258dup, NC_000019.10:g.14333242_14333258dup, NC_000019.10:g.14333241_14333258dup, NC_000019.10:g.14333240_14333258dup, NC_000019.10:g.14333239_14333258dup, NC_000019.10:g.14333238_14333258dup, NC_000019.10:g.14333237_14333258dup, NC_000019.10:g.14333236_14333258dup, NC_000019.10:g.14333234_14333258dup, NC_000019.10:g.14333258_14333259insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000019.9:g.14444053_14444070del, NC_000019.9:g.14444057_14444070del, NC_000019.9:g.14444058_14444070del, NC_000019.9:g.14444059_14444070del, NC_000019.9:g.14444060_14444070del, NC_000019.9:g.14444061_14444070del, NC_000019.9:g.14444062_14444070del, NC_000019.9:g.14444063_14444070del, NC_000019.9:g.14444064_14444070del, NC_000019.9:g.14444065_14444070del, NC_000019.9:g.14444066_14444070del, NC_000019.9:g.14444067_14444070del, NC_000019.9:g.14444068_14444070del, NC_000019.9:g.14444069_14444070del, NC_000019.9:g.14444070del, NC_000019.9:g.14444070dup, NC_000019.9:g.14444069_14444070dup, NC_000019.9:g.14444068_14444070dup, NC_000019.9:g.14444067_14444070dup, NC_000019.9:g.14444066_14444070dup, NC_000019.9:g.14444065_14444070dup, NC_000019.9:g.14444064_14444070dup, NC_000019.9:g.14444063_14444070dup, NC_000019.9:g.14444062_14444070dup, NC_000019.9:g.14444061_14444070dup, NC_000019.9:g.14444060_14444070dup, NC_000019.9:g.14444059_14444070dup, NC_000019.9:g.14444058_14444070dup, NC_000019.9:g.14444057_14444070dup, NC_000019.9:g.14444056_14444070dup, NC_000019.9:g.14444055_14444070dup, NC_000019.9:g.14444054_14444070dup, NC_000019.9:g.14444053_14444070dup, NC_000019.9:g.14444052_14444070dup, NC_000019.9:g.14444051_14444070dup, NC_000019.9:g.14444050_14444070dup, NC_000019.9:g.14444049_14444070dup, NC_000019.9:g.14444048_14444070dup, NC_000019.9:g.14444046_14444070dup, NC_000019.9:g.14444070_14444071insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

    2.

    rs1491508062 has merged into rs71164244 [Homo sapiens]
      Variant type:
      DELINS
      Alleles:
      AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
      Chromosome:
      19:14334368 (GRCh38)
      19:14445180 (GRCh37)
      Canonical SPDI:
      NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
      Gene:
      LINC01842 (Varview), LINC01841 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by alfa,by cluster
      MAF:
      AAAAAAAAAAAA=0./0 (ALFA)
      HGVS:
      NC_000019.10:g.14334368_14334380del, NC_000019.10:g.14334369_14334380del, NC_000019.10:g.14334370_14334380del, NC_000019.10:g.14334371_14334380del, NC_000019.10:g.14334372_14334380del, NC_000019.10:g.14334373_14334380del, NC_000019.10:g.14334374_14334380del, NC_000019.10:g.14334375_14334380del, NC_000019.10:g.14334376_14334380del, NC_000019.10:g.14334377_14334380del, NC_000019.10:g.14334378_14334380del, NC_000019.10:g.14334379_14334380del, NC_000019.10:g.14334380del, NC_000019.10:g.14334380dup, NC_000019.10:g.14334379_14334380dup, NC_000019.10:g.14334378_14334380dup, NC_000019.10:g.14334377_14334380dup, NC_000019.10:g.14334375_14334380dup, NC_000019.10:g.14334370_14334380dup, NC_000019.10:g.14334368_14334380dup, NC_000019.9:g.14445180_14445192del, NC_000019.9:g.14445181_14445192del, NC_000019.9:g.14445182_14445192del, NC_000019.9:g.14445183_14445192del, NC_000019.9:g.14445184_14445192del, NC_000019.9:g.14445185_14445192del, NC_000019.9:g.14445186_14445192del, NC_000019.9:g.14445187_14445192del, NC_000019.9:g.14445188_14445192del, NC_000019.9:g.14445189_14445192del, NC_000019.9:g.14445190_14445192del, NC_000019.9:g.14445191_14445192del, NC_000019.9:g.14445192del, NC_000019.9:g.14445192dup, NC_000019.9:g.14445191_14445192dup, NC_000019.9:g.14445190_14445192dup, NC_000019.9:g.14445189_14445192dup, NC_000019.9:g.14445187_14445192dup, NC_000019.9:g.14445182_14445192dup, NC_000019.9:g.14445180_14445192dup

      3.

      rs1491435519 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        AG>- [Show Flanks]
        Chromosome:
        19:14332498 (GRCh38)
        19:14443310 (GRCh37)
        Canonical SPDI:
        NC_000019.10:14332495:AGAG:AG
        Gene:
        LINC01842 (Varview), LINC01841 (Varview)
        Functional Consequence:
        2KB_upstream_variant,upstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa
        MAF:
        AGAG=0./0 (ALFA)
        -=0.000011/3 (TOPMED)
        HGVS:

        4.

        rs1491399018 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->G [Show Flanks]
          Chromosome:
          19:14332496 (GRCh38)
          19:14443309 (GRCh37)
          Canonical SPDI:
          NC_000019.10:14332496:G:GG
          Gene:
          LINC01842 (Varview), LINC01841 (Varview)
          Functional Consequence:
          2KB_upstream_variant,upstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          GG=0./0 (ALFA)
          G=0.000007/1 (GnomAD)
          HGVS:

          5.

          rs1491174639 [Homo sapiens]
            Variant type:
            DEL
            Alleles:
            CA>- [Show Flanks]
            Chromosome:
            19:14334355 (GRCh38)
            19:14445167 (GRCh37)
            Canonical SPDI:
            NC_000019.10:14334354:CA:
            Gene:
            LINC01842 (Varview), LINC01841 (Varview)
            Functional Consequence:
            intron_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            -=0.00034/4 (ALFA)
            -=0.00171/20 (TOMMO)
            HGVS:

            6.

            rs1491173561 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->GAAA [Show Flanks]
              Chromosome:
              19:14333232 (GRCh38)
              19:14444045 (GRCh37)
              Canonical SPDI:
              NC_000019.10:14333232:AAA:AAAGAAA
              Gene:
              LINC01842 (Varview), LINC01841 (Varview)
              Functional Consequence:
              2KB_upstream_variant,upstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              AAAGAAA=0./0 (ALFA)
              AAAG=0.00001/1 (GnomAD)
              AAAG=0.00009/1 (TOMMO)
              AAAG=0.00061/1 (Korea1K)
              HGVS:

              7.

              rs1491098076 has merged into rs145117206 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                AA>-,A,AAA [Show Flanks]
                Chromosome:
                19:14340495 (GRCh38)
                19:14451307 (GRCh37)
                Canonical SPDI:
                NC_000019.10:14340483:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000019.10:14340483:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:14340483:AAAAAAAAAAAAA:AAAAAAAAAAAAAA
                Gene:
                LINC01842 (Varview), LINC01841 (Varview)
                Functional Consequence:
                intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                AAAAAAAAAAAA=0./0 (ALFA)
                -=0.02745/14 (NorthernSweden)
                HGVS:

                8.

                rs1490950785 [Homo sapiens]
                  Variant type:
                  SNV:
                  Alleles:
                  G>T
                  Chromosome:
                  no mapping
                  Canonical SPDI:

                  9.

                  rs1490884170 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    C>G [Show Flanks]
                    Chromosome:
                    19:14336925 (GRCh38)
                    19:14447737 (GRCh37)
                    Canonical SPDI:
                    NC_000019.10:14336924:C:G
                    Gene:
                    LINC01842 (Varview), LINC01841 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    G=0.000071/1 (ALFA)
                    G=0.000004/1 (TOPMED)
                    G=0.000021/3 (GnomAD)
                    HGVS:

                    10.

                    rs1490605099 has merged into rs1048167001 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      AAAAA>-,A,AAAA,AAAAAA [Show Flanks]
                      Chromosome:
                      19:14338240 (GRCh38)
                      19:14449052 (GRCh37)
                      Canonical SPDI:
                      NC_000019.10:14338236:AAAAAAAA:AAA,NC_000019.10:14338236:AAAAAAAA:AAAA,NC_000019.10:14338236:AAAAAAAA:AAAAAAA,NC_000019.10:14338236:AAAAAAAA:AAAAAAAAA
                      Gene:
                      LINC01842 (Varview), LINC01841 (Varview)
                      Functional Consequence:
                      intron_variant
                      Validated:
                      by frequency,by alfa,by cluster
                      MAF:
                      AAAA=0./0 (ALFA)
                      -=0.000004/1 (TOPMED)
                      HGVS:

                      11.

                      rs1490294669 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        C>G,T [Show Flanks]
                        Chromosome:
                        19:14340216 (GRCh38)
                        19:14451028 (GRCh37)
                        Canonical SPDI:
                        NC_000019.10:14340215:C:G,NC_000019.10:14340215:C:T
                        Gene:
                        LINC01842 (Varview), LINC01841 (Varview)
                        Functional Consequence:
                        intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        T=0./0 (ALFA)
                        HGVS:

                        12.

                        rs1490133982 [Homo sapiens]
                          Variant type:
                          SNV
                          Alleles:
                          G>A [Show Flanks]
                          Chromosome:
                          19:14340368 (GRCh38)
                          19:14451180 (GRCh37)
                          Canonical SPDI:
                          NC_000019.10:14340367:G:A
                          Gene:
                          LINC01842 (Varview), LINC01841 (Varview)
                          Functional Consequence:
                          intron_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          A=0./0 (ALFA)
                          A=0.000007/1 (GnomAD)
                          A=0.000011/3 (TOPMED)
                          HGVS:

                          13.

                          rs1490067951 has merged into rs71164244 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            AAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
                            Chromosome:
                            19:14334368 (GRCh38)
                            19:14445180 (GRCh37)
                            Canonical SPDI:
                            NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000019.10:14334355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
                            Gene:
                            LINC01842 (Varview), LINC01841 (Varview)
                            Functional Consequence:
                            intron_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            AAAAAAAAAAAA=0./0 (ALFA)
                            HGVS:
                            NC_000019.10:g.14334368_14334380del, NC_000019.10:g.14334369_14334380del, NC_000019.10:g.14334370_14334380del, NC_000019.10:g.14334371_14334380del, NC_000019.10:g.14334372_14334380del, NC_000019.10:g.14334373_14334380del, NC_000019.10:g.14334374_14334380del, NC_000019.10:g.14334375_14334380del, NC_000019.10:g.14334376_14334380del, NC_000019.10:g.14334377_14334380del, NC_000019.10:g.14334378_14334380del, NC_000019.10:g.14334379_14334380del, NC_000019.10:g.14334380del, NC_000019.10:g.14334380dup, NC_000019.10:g.14334379_14334380dup, NC_000019.10:g.14334378_14334380dup, NC_000019.10:g.14334377_14334380dup, NC_000019.10:g.14334375_14334380dup, NC_000019.10:g.14334370_14334380dup, NC_000019.10:g.14334368_14334380dup, NC_000019.9:g.14445180_14445192del, NC_000019.9:g.14445181_14445192del, NC_000019.9:g.14445182_14445192del, NC_000019.9:g.14445183_14445192del, NC_000019.9:g.14445184_14445192del, NC_000019.9:g.14445185_14445192del, NC_000019.9:g.14445186_14445192del, NC_000019.9:g.14445187_14445192del, NC_000019.9:g.14445188_14445192del, NC_000019.9:g.14445189_14445192del, NC_000019.9:g.14445190_14445192del, NC_000019.9:g.14445191_14445192del, NC_000019.9:g.14445192del, NC_000019.9:g.14445192dup, NC_000019.9:g.14445191_14445192dup, NC_000019.9:g.14445190_14445192dup, NC_000019.9:g.14445189_14445192dup, NC_000019.9:g.14445187_14445192dup, NC_000019.9:g.14445182_14445192dup, NC_000019.9:g.14445180_14445192dup

                            14.

                            rs1490067471 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              G>A,C,T [Show Flanks]
                              Chromosome:
                              19:14338049 (GRCh38)
                              19:14448861 (GRCh37)
                              Canonical SPDI:
                              NC_000019.10:14338048:G:A,NC_000019.10:14338048:G:C,NC_000019.10:14338048:G:T
                              Gene:
                              LINC01842 (Varview), LINC01841 (Varview)
                              Functional Consequence:
                              intron_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              C=0./0 (ALFA)
                              A=0.00004/1 (TOMMO)
                              HGVS:

                              15.

                              rs1489962303 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                G>C [Show Flanks]
                                Chromosome:
                                19:14341214 (GRCh38)
                                19:14452026 (GRCh37)
                                Canonical SPDI:
                                NC_000019.10:14341213:G:C
                                Gene:
                                LINC01842 (Varview), LINC01841 (Varview)
                                Functional Consequence:
                                intron_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                C=0./0 (ALFA)
                                C=0.000004/1 (TOPMED)
                                C=0.000014/2 (GnomAD)
                                HGVS:

                                16.

                                rs1489905123 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  19:14339091 (GRCh38)
                                  19:14449903 (GRCh37)
                                  Canonical SPDI:
                                  NC_000019.10:14339090:C:T
                                  Gene:
                                  LINC01842 (Varview), LINC01841 (Varview)
                                  Functional Consequence:
                                  intron_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  T=0.000071/1 (ALFA)
                                  T=0.000064/9 (GnomAD)
                                  T=0.000071/1 (TOMMO)
                                  T=0.000076/20 (TOPMED)
                                  T=0.000342/1 (KOREAN)
                                  HGVS:

                                  17.

                                  rs1489898120 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    T>C [Show Flanks]
                                    Chromosome:
                                    19:14333307 (GRCh38)
                                    19:14444119 (GRCh37)
                                    Canonical SPDI:
                                    NC_000019.10:14333306:T:C
                                    Gene:
                                    LINC01842 (Varview), LINC01841 (Varview)
                                    Functional Consequence:
                                    2KB_upstream_variant,upstream_transcript_variant,intron_variant
                                    Validated:
                                    by frequency,by alfa
                                    MAF:
                                    C=0./0 (ALFA)
                                    HGVS:

                                    18.

                                    rs1489194506 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      A>G [Show Flanks]
                                      Chromosome:
                                      19:14341640 (GRCh38)
                                      19:14452452 (GRCh37)
                                      Canonical SPDI:
                                      NC_000019.10:14341639:A:G
                                      Gene:
                                      LINC01842 (Varview), LINC01841 (Varview)
                                      Functional Consequence:
                                      intron_variant
                                      Validated:
                                      by frequency,by alfa
                                      MAF:
                                      G=0./0 (ALFA)
                                      G=0.000004/1 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1489129912 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        C>G [Show Flanks]
                                        Chromosome:
                                        19:14340334 (GRCh38)
                                        19:14451146 (GRCh37)
                                        Canonical SPDI:
                                        NC_000019.10:14340333:C:G
                                        Gene:
                                        LINC01842 (Varview), LINC01841 (Varview)
                                        Functional Consequence:
                                        intron_variant
                                        Validated:
                                        by frequency,by alfa,by cluster
                                        MAF:
                                        G=0./0 (ALFA)
                                        G=0.000007/1 (GnomAD)
                                        G=0.000008/2 (TOPMED)
                                        HGVS:

                                        20.

                                        rs1489071689 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          A>T [Show Flanks]
                                          Chromosome:
                                          19:14334043 (GRCh38)
                                          19:14444855 (GRCh37)
                                          Canonical SPDI:
                                          NC_000019.10:14334042:A:T
                                          Gene:
                                          LINC01842 (Varview), LINC01841 (Varview)
                                          Functional Consequence:
                                          intron_variant
                                          Validated:
                                          by frequency
                                          MAF:
                                          T=0.00006/1 (GnomAD)
                                          HGVS:

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