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Items: 1 to 20 of 1000

1.

rs1491575021 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    AT>- [Show Flanks]
    Chromosome:
    11:5623127 (GRCh38)
    11:5644357 (GRCh37)
    Canonical SPDI:
    NC_000011.10:5623125:TAT:T
    Gene:
    TRIM34 (Varview), TRIM5 (Varview), TRIM6-TRIM34 (Varview)
    Functional Consequence:
    genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
    Validated:
    by frequency,by alfa
    MAF:
    T=0./0 (ALFA)
    HGVS:

    2.

    rs1491539428 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      TT>- [Show Flanks]
      Chromosome:
      11:5675205 (GRCh38)
      11:5696435 (GRCh37)
      Canonical SPDI:
      NC_000011.10:5675204:TT:
      Gene:
      TRIM5 (Varview)
      Functional Consequence:
      intron_variant
      Validated:
      by frequency,by cluster
      MAF:
      -=0.055/204 (TWINSUK)
      -=0.0698/269 (ALSPAC)
      HGVS:

      3.

      rs1491528573 [Homo sapiens]
        Variant type:
        DELINS
        Alleles:
        ->GA [Show Flanks]
        Chromosome:
        11:5592932 (GRCh38)
        11:5614163 (GRCh37)
        Canonical SPDI:
        NC_000011.10:5592932:A:AGA
        Gene:
        TRIM5 (Varview)
        Functional Consequence:
        intron_variant,genic_downstream_transcript_variant
        Validated:
        by frequency,by alfa
        MAF:
        AGA=0./0 (ALFA)
        AG=0.000079/8 (GnomAD)
        HGVS:

        4.

        rs1491525050 [Homo sapiens]
          Variant type:
          DELINS
          Alleles:
          ->CTT [Show Flanks]
          Chromosome:
          11:5633147 (GRCh38)
          11:5654378 (GRCh37)
          Canonical SPDI:
          NC_000011.10:5633147:TT:TTCTT
          Gene:
          TRIM34 (Varview), TRIM5 (Varview), TRIM6-TRIM34 (Varview)
          Functional Consequence:
          genic_downstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa
          MAF:
          TTCTT=0./0 (ALFA)
          TTC=0.000008/2 (TOPMED)
          HGVS:

          5.

          rs1491511874 has merged into rs67834754 [Homo sapiens]
            Variant type:
            DELINS
            Alleles:
            G>-,GG [Show Flanks]
            Chromosome:
            11:5591896 (GRCh38)
            11:5613126 (GRCh37)
            Canonical SPDI:
            NC_000011.10:5591895:GGGGGG:GGGGG,NC_000011.10:5591895:GGGGGG:GGGGGGG
            Gene:
            TRIM5 (Varview)
            Functional Consequence:
            intron_variant,genic_downstream_transcript_variant
            Validated:
            by frequency,by alfa,by cluster
            MAF:
            GGGGGGG=0./0 (ALFA)
            HGVS:

            6.

            rs1491498839 [Homo sapiens]
              Variant type:
              DELINS
              Alleles:
              ->CACACACACACACACACACACACACACATATA,CACACACACACACACACACACACACATATA,CACACACACACACACACACACACATA,CACACACACACACACACACACATA,CACACACACACACACACACACATATA,CACACACACACACACACACATA,CACACACACACACACACACATATA,CACACACACACACACACATA,CACACACACACACACACATATA,CACACACACACACACACATATATA,CACACACACACACACACATATATATA,CACACACACACACACATA,CACACACACACACACATATA,CACACACACACACACATATATA,CACACACACACACACATATATATA,CACACACACACACATA,CACACACACACACATACACACACATATATATA,CACACACACACACATATA,CACACACACACACATATATA,CACACACACACACATATATATA,CACACACACACAGATATA,CACACACACACATA,CACACACACACATATA,CACACACACACATATATA,CACACACACACATATATATA,CACACACACACATATATATATA,CACACACACATA,CACACACACATATA,CACACACACATATATA,CACACACACATATATATA,CACACACACATATATATATA,CACACACACATATATATATATA,CACACACATA,CACACACATATA,CACACACATATATA,CACACACATATATATA,CACACACATATATATATA,CACACACATATATATATATATATATA,CACACATA,CACACATATA,CACACATATATA,CACACATATATATA,CACACATATATATATA,CACACATATATATATATATA,CACACATATATATATATATATA,CACACATATATATATATATATATA,CACACATATATATATATATATATATA,CACACATATATATATATATATATATATA,CACACATATATATATATATATATATATATA,CACATA,CACATATA,CACATATATA,CACATATATATA,CACATATATATATA,CACATATATATATATATA,CACATATATATATATATATA,CACATATATATATATATATATA,CACATATATATATATATATATATA,CACATATATATATATATATATATATA,CACATATATATATATATATATATATATA,CACATATATATATATATATATATATATATA,CACATATATATATATATATATATATATATATA,CACATATATATATATATATATATATATATATATA,CATA,CATATA,CATATATA,CATATATATA,CATATATATATATA,CATATATATATATATATA,CATATATATATATATATATA,CATATATATATATATATATATA,CATATATATATATATATATATATA,CATATATATATATATATATATATATA,CATATATATATATATATATATATATATA,CATATATATATATATATATATATATATATA,CATATATATATATATATATATATATATATATA,CATATATATATATATATATATATATATATATATA [Show Flanks]
              Chromosome:
              11:5634530 (GRCh38)
              11:5655761 (GRCh37)
              Canonical SPDI:
              NC_000011.10:5634530:A:ACACACACACACACACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACACACATATATA,NC_000011.10:5634530:A:ACACACACACACACACACATATATATA,NC_000011.10:5634530:A:ACACACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACACATATATA,NC_000011.10:5634530:A:ACACACACACACACACATATATATA,NC_000011.10:5634530:A:ACACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACACATACACACACATATATATA,NC_000011.10:5634530:A:ACACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACACATATATA,NC_000011.10:5634530:A:ACACACACACACACATATATATA,NC_000011.10:5634530:A:ACACACACACACAGATATA,NC_000011.10:5634530:A:ACACACACACACATA,NC_000011.10:5634530:A:ACACACACACACATATA,NC_000011.10:5634530:A:ACACACACACACATATATA,NC_000011.10:5634530:A:ACACACACACACATATATATA,NC_000011.10:5634530:A:ACACACACACACATATATATATA,NC_000011.10:5634530:A:ACACACACACATA,NC_000011.10:5634530:A:ACACACACACATATA,NC_000011.10:5634530:A:ACACACACACATATATA,NC_000011.10:5634530:A:ACACACACACATATATATA,NC_000011.10:5634530:A:ACACACACACATATATATATA,NC_000011.10:5634530:A:ACACACACACATATATATATATA,NC_000011.10:5634530:A:ACACACACATA,NC_000011.10:5634530:A:ACACACACATATA,NC_000011.10:5634530:A:ACACACACATATATA,NC_000011.10:5634530:A:ACACACACATATATATA,NC_000011.10:5634530:A:ACACACACATATATATATA,NC_000011.10:5634530:A:ACACACACATATATATATATATATATA,NC_000011.10:5634530:A:ACACACATA,NC_000011.10:5634530:A:ACACACATATA,NC_000011.10:5634530:A:ACACACATATATA,NC_000011.10:5634530:A:ACACACATATATATA,NC_000011.10:5634530:A:ACACACATATATATATA,NC_000011.10:5634530:A:ACACACATATATATATATATA,NC_000011.10:5634530:A:ACACACATATATATATATATATA,NC_000011.10:5634530:A:ACACACATATATATATATATATATA,NC_000011.10:5634530:A:ACACACATATATATATATATATATATA,NC_000011.10:5634530:A:ACACACATATATATATATATATATATATA,NC_000011.10:5634530:A:ACACACATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACACATA,NC_000011.10:5634530:A:ACACATATA,NC_000011.10:5634530:A:ACACATATATA,NC_000011.10:5634530:A:ACACATATATATA,NC_000011.10:5634530:A:ACACATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACACATATATATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACATA,NC_000011.10:5634530:A:ACATATA,NC_000011.10:5634530:A:ACATATATA,NC_000011.10:5634530:A:ACATATATATA,NC_000011.10:5634530:A:ACATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATATATATATATA,NC_000011.10:5634530:A:ACATATATATATATATATATATATATATATATATA
              Gene:
              TRIM34 (Varview), TRIM5 (Varview), TRIM6-TRIM34 (Varview)
              Functional Consequence:
              genic_downstream_transcript_variant,intron_variant
              Validated:
              by frequency,by alfa,by cluster
              MAF:
              ACACACACACACACACACACATATA=0./0 (ALFA)
              ACACATATATATAT=0.000004/1 (TOPMED)
              HGVS:
              NC_000011.10:g.5634531AC[14]AT[2]A[1], NC_000011.10:g.5634531AC[13]AT[2]A[1], NC_000011.10:g.5634531AC[12]ATA[1], NC_000011.10:g.5634531AC[11]ATA[1], NC_000011.10:g.5634531AC[11]AT[2]A[1], NC_000011.10:g.5634531AC[10]ATA[1], NC_000011.10:g.5634531AC[10]AT[2]A[1], NC_000011.10:g.5634531AC[9]ATA[1], NC_000011.10:g.5634531AC[9]AT[2]A[1], NC_000011.10:g.5634531AC[9]AT[3]A[1], NC_000011.10:g.5634531AC[9]AT[4]A[1], NC_000011.10:g.5634531AC[8]ATA[1], NC_000011.10:g.5634531AC[8]AT[2]A[1], NC_000011.10:g.5634531AC[8]AT[3]A[1], NC_000011.10:g.5634531AC[8]AT[4]A[1], NC_000011.10:g.5634531AC[7]ATA[1], NC_000011.10:g.5634531AC[7]ATACACACACATATATATA[1], NC_000011.10:g.5634531AC[7]AT[2]A[1], NC_000011.10:g.5634531AC[7]AT[3]A[1], NC_000011.10:g.5634531AC[7]AT[4]A[1], NC_000011.10:g.5634531AC[6]AGATATA[1], NC_000011.10:g.5634531AC[6]ATA[1], NC_000011.10:g.5634531AC[6]AT[2]A[1], NC_000011.10:g.5634531AC[6]AT[3]A[1], NC_000011.10:g.5634531AC[6]AT[4]A[1], NC_000011.10:g.5634531AC[6]AT[5]A[1], NC_000011.10:g.5634531AC[5]ATA[1], NC_000011.10:g.5634531AC[5]AT[2]A[1], NC_000011.10:g.5634531AC[5]AT[3]A[1], NC_000011.10:g.5634531AC[5]AT[4]A[1], NC_000011.10:g.5634531AC[5]AT[5]A[1], NC_000011.10:g.5634531AC[5]AT[6]A[1], NC_000011.10:g.5634531AC[4]ATA[1], NC_000011.10:g.5634531AC[4]AT[2]A[1], NC_000011.10:g.5634531AC[4]AT[3]A[1], NC_000011.10:g.5634531AC[4]AT[4]A[1], NC_000011.10:g.5634531AC[4]AT[5]A[1], NC_000011.10:g.5634531AC[4]AT[9]A[1], NC_000011.10:g.5634531AC[3]ATA[1], NC_000011.10:g.5634531AC[3]AT[2]A[1], NC_000011.10:g.5634531AC[3]AT[3]A[1], NC_000011.10:g.5634531AC[3]AT[4]A[1], NC_000011.10:g.5634531AC[3]AT[5]A[1], NC_000011.10:g.5634531AC[3]AT[7]A[1], NC_000011.10:g.5634531AC[3]AT[8]A[1], NC_000011.10:g.5634531AC[3]AT[9]A[1], NC_000011.10:g.5634531AC[3]AT[10]A[1], NC_000011.10:g.5634531AC[3]AT[11]A[1], NC_000011.10:g.5634531AC[3]AT[12]A[1], NC_000011.10:g.5634531AC[2]ATA[1], NC_000011.10:g.5634531AC[2]AT[2]A[1], NC_000011.10:g.5634531AC[2]AT[3]A[1], NC_000011.10:g.5634531AC[2]AT[4]A[1], NC_000011.10:g.5634531AC[2]AT[5]A[1], NC_000011.10:g.5634531AC[2]AT[7]A[1], NC_000011.10:g.5634531AC[2]AT[8]A[1], NC_000011.10:g.5634531AC[2]AT[9]A[1], NC_000011.10:g.5634531AC[2]AT[10]A[1], NC_000011.10:g.5634531AC[2]AT[11]A[1], NC_000011.10:g.5634531AC[2]AT[12]A[1], NC_000011.10:g.5634531AC[2]AT[13]A[1], NC_000011.10:g.5634531AC[2]AT[14]A[1], NC_000011.10:g.5634531AC[2]AT[15]A[1], NC_000011.10:g.5634531_5634532insCATA, NC_000011.10:g.5634531_5634532insCATATA, NC_000011.10:g.5634531_5634532insCATATATA, NC_000011.10:g.5634531_5634532insCATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATATATATATATA, NC_000011.10:g.5634531_5634532insCATATATATATATATATATATATATATATATATA, NC_000011.9:g.5655761AC[14]AT[2]A[1], NC_000011.9:g.5655761AC[13]AT[2]A[1], NC_000011.9:g.5655761AC[12]ATA[1], NC_000011.9:g.5655761AC[11]ATA[1], NC_000011.9:g.5655761AC[11]AT[2]A[1], NC_000011.9:g.5655761AC[10]ATA[1], NC_000011.9:g.5655761AC[10]AT[2]A[1], NC_000011.9:g.5655761AC[9]ATA[1], NC_000011.9:g.5655761AC[9]AT[2]A[1], NC_000011.9:g.5655761AC[9]AT[3]A[1], NC_000011.9:g.5655761AC[9]AT[4]A[1], NC_000011.9:g.5655761AC[8]ATA[1], NC_000011.9:g.5655761AC[8]AT[2]A[1], NC_000011.9:g.5655761AC[8]AT[3]A[1], NC_000011.9:g.5655761AC[8]AT[4]A[1], NC_000011.9:g.5655761AC[7]ATA[1], NC_000011.9:g.5655761AC[7]ATACACACACATATATATA[1], NC_000011.9:g.5655761AC[7]AT[2]A[1], NC_000011.9:g.5655761AC[7]AT[3]A[1], NC_000011.9:g.5655761AC[7]AT[4]A[1], NC_000011.9:g.5655761AC[6]AGATATA[1], NC_000011.9:g.5655761AC[6]ATA[1], NC_000011.9:g.5655761AC[6]AT[2]A[1], NC_000011.9:g.5655761AC[6]AT[3]A[1], NC_000011.9:g.5655761AC[6]AT[4]A[1], NC_000011.9:g.5655761AC[6]AT[5]A[1], NC_000011.9:g.5655761AC[5]ATA[1], NC_000011.9:g.5655761AC[5]AT[2]A[1], NC_000011.9:g.5655761AC[5]AT[3]A[1], NC_000011.9:g.5655761AC[5]AT[4]A[1], NC_000011.9:g.5655761AC[5]AT[5]A[1], NC_000011.9:g.5655761AC[5]AT[6]A[1], NC_000011.9:g.5655761AC[4]ATA[1], NC_000011.9:g.5655761AC[4]AT[2]A[1], NC_000011.9:g.5655761AC[4]AT[3]A[1], NC_000011.9:g.5655761AC[4]AT[4]A[1], NC_000011.9:g.5655761AC[4]AT[5]A[1], NC_000011.9:g.5655761AC[4]AT[9]A[1], NC_000011.9:g.5655761AC[3]ATA[1], NC_000011.9:g.5655761AC[3]AT[2]A[1], NC_000011.9:g.5655761AC[3]AT[3]A[1], NC_000011.9:g.5655761AC[3]AT[4]A[1], NC_000011.9:g.5655761AC[3]AT[5]A[1], NC_000011.9:g.5655761AC[3]AT[7]A[1], NC_000011.9:g.5655761AC[3]AT[8]A[1], NC_000011.9:g.5655761AC[3]AT[9]A[1], NC_000011.9:g.5655761AC[3]AT[10]A[1], NC_000011.9:g.5655761AC[3]AT[11]A[1], NC_000011.9:g.5655761AC[3]AT[12]A[1], NC_000011.9:g.5655761AC[2]ATA[1], NC_000011.9:g.5655761AC[2]AT[2]A[1], NC_000011.9:g.5655761AC[2]AT[3]A[1], NC_000011.9:g.5655761AC[2]AT[4]A[1], NC_000011.9:g.5655761AC[2]AT[5]A[1], NC_000011.9:g.5655761AC[2]AT[7]A[1], NC_000011.9:g.5655761AC[2]AT[8]A[1], NC_000011.9:g.5655761AC[2]AT[9]A[1], NC_000011.9:g.5655761AC[2]AT[10]A[1], NC_000011.9:g.5655761AC[2]AT[11]A[1], NC_000011.9:g.5655761AC[2]AT[12]A[1], NC_000011.9:g.5655761AC[2]AT[13]A[1], NC_000011.9:g.5655761AC[2]AT[14]A[1], NC_000011.9:g.5655761AC[2]AT[15]A[1], NC_000011.9:g.5655761_5655762insCATA, NC_000011.9:g.5655761_5655762insCATATA, NC_000011.9:g.5655761_5655762insCATATATA, NC_000011.9:g.5655761_5655762insCATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATATATATATATA, NC_000011.9:g.5655761_5655762insCATATATATATATATATATATATATATATATATA

              7.

              rs1491463066 has merged into rs1305516695 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                ATAT>-,AT,ATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT [Show Flanks]
                Chromosome:
                11:5657604 (GRCh38)
                11:5678834 (GRCh37)
                Canonical SPDI:
                NC_000011.10:5657599:ATATATAT:ATAT,NC_000011.10:5657599:ATATATAT:ATATAT,NC_000011.10:5657599:ATATATAT:ATATATATAT,NC_000011.10:5657599:ATATATAT:ATATATATATATATATATAT,NC_000011.10:5657599:ATATATAT:ATATATATATATATATATATAT,NC_000011.10:5657599:ATATATAT:ATATATATATATATATATATATAT
                Gene:
                TRIM5 (Varview), LOC107984302 (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                ATATAT=0./0 (ALFA)
                ATATATATATATAT=0.000004/1 (TOPMED)
                HGVS:

                8.

                rs1491453895 [Homo sapiens]
                  Variant type:
                  DELINS
                  Alleles:
                  AA>- [Show Flanks]
                  Chromosome:
                  11:5657707 (GRCh38)
                  11:5678937 (GRCh37)
                  Canonical SPDI:
                  NC_000011.10:5657705:AAA:A
                  Gene:
                  TRIM5 (Varview), LOC107984302 (Varview)
                  Functional Consequence:
                  intron_variant,genic_downstream_transcript_variant
                  Validated:
                  by frequency,by alfa
                  MAF:
                  A=0.000084/1 (ALFA)
                  -=0.000033/4 (GnomAD)
                  HGVS:

                  9.

                  rs1491445909 has merged into rs370297403 [Homo sapiens]
                    Variant type:
                    DELINS
                    Alleles:
                    AT>-,ATAT [Show Flanks]
                    Chromosome:
                    11:5675207 (GRCh38)
                    11:5696437 (GRCh37)
                    Canonical SPDI:
                    NC_000011.10:5675205:TAT:T,NC_000011.10:5675205:TAT:TATAT
                    Gene:
                    TRIM5 (Varview)
                    Functional Consequence:
                    intron_variant
                    Validated:
                    by frequency,by alfa,by cluster
                    MAF:
                    T=0.098959/1616 (ALFA)
                    -=0.056945/255 (Estonian)
                    -=0.111667/67 (NorthernSweden)
                    -=0.128359/17872 (GnomAD)
                    -=0.15038/39804 (TOPMED)
                    -=0.229633/1150 (1000Genomes)
                    -=0.422818/7086 (TOMMO)
                    -=0.424672/778 (Korea1K)
                    HGVS:

                    10.

                    rs1491431871 has merged into rs869222613 [Homo sapiens]
                      Variant type:
                      DELINS
                      Alleles:
                      CT>-,CTCT [Show Flanks]
                      Chromosome:
                      11:5613909 (GRCh38)
                      11:5635139 (GRCh37)
                      Canonical SPDI:
                      NC_000011.10:5613907:TCT:T,NC_000011.10:5613907:TCT:TCTCT
                      Gene:
                      TRIM5 (Varview), TRIM6-TRIM34 (Varview)
                      Functional Consequence:
                      intron_variant,genic_downstream_transcript_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      -=0.0002/1 (GnomAD)
                      HGVS:

                      11.

                      rs1491396605 [Homo sapiens]
                        Variant type:
                        DELINS
                        Alleles:
                        ->G [Show Flanks]
                        Chromosome:
                        11:5604782 (GRCh38)
                        11:5626013 (GRCh37)
                        Canonical SPDI:
                        NC_000011.10:5604782:GGGGG:GGGGGG
                        Gene:
                        TRIM5 (Varview), TRIM6 (Varview), TRIM6-TRIM34 (Varview)
                        Functional Consequence:
                        intron_variant,genic_downstream_transcript_variant
                        Validated:
                        by frequency,by alfa
                        MAF:
                        GGGGGG=0./0 (ALFA)
                        G=0.000008/2 (TOPMED)
                        HGVS:

                        12.

                        rs1491380755 [Homo sapiens]
                          Variant type:
                          DEL
                          Alleles:
                          AA>- [Show Flanks]
                          Chromosome:
                          11:5657675 (GRCh38)
                          11:5678905 (GRCh37)
                          Canonical SPDI:
                          NC_000011.10:5657674:AA:
                          Gene:
                          TRIM5 (Varview), LOC107984302 (Varview)
                          Functional Consequence:
                          intron_variant,genic_downstream_transcript_variant
                          Validated:
                          by frequency,by alfa,by cluster
                          MAF:
                          -=0./0 (ALFA)
                          -=0.00099/16 (TOMMO)
                          -=0.00297/5 (Korea1K)
                          -=0.01292/7 (NorthernSweden)
                          -=0.01298/65 (1000Genomes)
                          -=0.02762/2270 (GnomAD)
                          HGVS:

                          13.

                          rs1491377402 has merged into rs35793386 [Homo sapiens]
                            Variant type:
                            DELINS
                            Alleles:
                            TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
                            Chromosome:
                            11:5595732 (GRCh38)
                            11:5616962 (GRCh37)
                            Canonical SPDI:
                            NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:5595720:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
                            Gene:
                            TRIM5 (Varview), TRIM6 (Varview), TRIM6-TRIM34 (Varview)
                            Functional Consequence:
                            intron_variant,2KB_upstream_variant,genic_downstream_transcript_variant,upstream_transcript_variant
                            Validated:
                            by frequency,by alfa,by cluster
                            MAF:
                            TTTTTTTTTTTTT=0./0 (ALFA)
                            -=0.000004/1 (TOPMED)
                            TT=0.197324/118 (NorthernSweden)
                            HGVS:

                            14.

                            rs1491365580 [Homo sapiens]
                              Variant type:
                              DEL
                              Alleles:
                              AA>- [Show Flanks]
                              Chromosome:
                              11:5657697 (GRCh38)
                              11:5678927 (GRCh37)
                              Canonical SPDI:
                              NC_000011.10:5657696:AA:
                              Gene:
                              TRIM5 (Varview), LOC107984302 (Varview)
                              Functional Consequence:
                              intron_variant,genic_downstream_transcript_variant
                              Validated:
                              by frequency,by alfa,by cluster
                              MAF:
                              -=0./0 (ALFA)
                              -=0.000004/1 (TOPMED)
                              -=0.000008/1 (GnomAD)
                              HGVS:

                              15.

                              rs1491357807 [Homo sapiens]
                                Variant type:
                                DEL
                                Alleles:
                                AA>- [Show Flanks]
                                Chromosome:
                                11:5657599 (GRCh38)
                                11:5678829 (GRCh37)
                                Canonical SPDI:
                                NC_000011.10:5657598:AA:
                                Gene:
                                TRIM5 (Varview), LOC107984302 (Varview)
                                Functional Consequence:
                                intron_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                -=0./0 (ALFA)
                                -=0.00021/4 (TOMMO)
                                -=0.00369/326 (GnomAD)
                                HGVS:

                                16.

                                rs1491343105 has merged into rs34443439 [Homo sapiens]
                                  Variant type:
                                  DELINS
                                  Alleles:
                                  TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTTTTTTT [Show Flanks]
                                  Chromosome:
                                  11:5656367 (GRCh38)
                                  11:5677597 (GRCh37)
                                  Canonical SPDI:
                                  NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000011.10:5656355:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT
                                  Gene:
                                  TRIM5 (Varview), LOC107984302 (Varview)
                                  Functional Consequence:
                                  intron_variant,genic_downstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa,by cluster
                                  MAF:
                                  TTTTTTTTTTTTT=0./0 (ALFA)
                                  -=0.2468/1236 (1000Genomes)
                                  HGVS:

                                  17.

                                  rs1491320474 [Homo sapiens]
                                    Variant type:
                                    DELINS
                                    Alleles:
                                    ->TTATATATTATATATAATGCATTATATAT [Show Flanks]
                                    Chromosome:
                                    11:5657600 (GRCh38)
                                    11:5678831 (GRCh37)
                                    Canonical SPDI:
                                    NC_000011.10:5657600:TATATATTTATATATTATATATAATGCATTATATAT:TATATATTTATATATTATATATAATGCATTATATATTTATATATTATATATAATGCATTATATAT
                                    Gene:
                                    TRIM5 (Varview), LOC107984302 (Varview)
                                    Functional Consequence:
                                    intron_variant,genic_downstream_transcript_variant
                                    Validated:
                                    by frequency,by cluster
                                    MAF:
                                    TATATATTTATATATTATATATAATGCAT=0.00012/9 (GnomAD)
                                    TATATATTTATATATTATATATAATGCAT=0.00202/33 (TOMMO)
                                    HGVS:

                                    18.

                                    rs1491292378 has merged into rs745849246 [Homo sapiens]
                                      Variant type:
                                      DELINS
                                      Alleles:
                                      TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT [Show Flanks]
                                      Chromosome:
                                      11:5643134 (GRCh38)
                                      11:5664364 (GRCh37)
                                      Canonical SPDI:
                                      NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000011.10:5643125:TTTTTTTTTTT:TTTTTTTTTTTTTTTTT
                                      Gene:
                                      TRIM34 (Varview), TRIM5 (Varview), TRIM6-TRIM34 (Varview)
                                      Functional Consequence:
                                      intron_variant,genic_downstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      TTTTTTTTT=0./0 (ALFA)
                                      TTTTTT=0.000004/1 (TOPMED)
                                      -=0.159056/613 (ALSPAC)
                                      -=0.169364/628 (TWINSUK)
                                      HGVS:

                                      19.

                                      rs1491287606 [Homo sapiens]
                                        Variant type:
                                        INS
                                        Alleles:
                                        ->T [Show Flanks]
                                        Chromosome:
                                        11:5657697 (GRCh38)
                                        11:5678928 (GRCh37)
                                        Canonical SPDI:
                                        NC_000011.10:5657697::T
                                        Gene:
                                        TRIM5 (Varview), LOC107984302 (Varview)
                                        Functional Consequence:
                                        intron_variant,genic_downstream_transcript_variant
                                        Validated:
                                        by frequency,by alfa
                                        MAF:
                                        T=0./0 (ALFA)
                                        T=0.000009/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1491281812 [Homo sapiens]
                                          Variant type:
                                          INS
                                          Alleles:
                                          ->TATATTTAT,TATTTAT,TTTAT [Show Flanks]
                                          Chromosome:
                                          11:5657706 (GRCh38)
                                          11:5678937 (GRCh37)
                                          Canonical SPDI:
                                          NC_000011.10:5657706::TATATTTAT,NC_000011.10:5657706::TATTTAT,NC_000011.10:5657706::TTTAT
                                          Gene:
                                          TRIM5 (Varview), LOC107984302 (Varview)
                                          Functional Consequence:
                                          intron_variant,genic_downstream_transcript_variant
                                          Validated:
                                          by cluster
                                          HGVS:

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