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Items: 1 to 20 of 247

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054280inversion1nstd229human GRCh38 chr7: 128,104,928-130,077,832 , GRCh37.p13 chr7: 127,744,980-129,717,672 CICP14, RNA5SP243, 63 more genes
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6838056copy number variation1nstd229human GRCh38 chr7: 128,531,484-128,767,012 , GRCh37.p13 chr7: 128,171,538-128,407,066 GARIN1A, RPS10P15, 9 more genes
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6837736copy number variation1nstd229human GRCh38 chr7: 128,633,501-128,974,300 , GRCh37.p13 chr7: 128,273,555-128,614,354 FLNC, KCP, 20 more genes
    nsv6832385copy number variation1nstd229human GRCh38 chr7: 128,700,777-128,701,457 , GRCh37.p13 chr7: 128,340,831-128,341,511 GARIN1A
    nsv6831626copy number variation1nstd229human GRCh38 chr7: 128,692,185-128,697,432 , GRCh37.p13 chr7: 128,332,239-128,337,486 RNA5SP242, IMP3P2, 2 more genes
    nsv6824012copy number variation1nstd229human GRCh38 chr7: 128,566,349-128,751,121 , GRCh37.p13 chr7: 128,206,403-128,391,175 RNU6-177P, GARIN1B, 8 more genes
    nsv6823019copy number variation1nstd229human GRCh38 chr7: 128,692,114-128,692,509 , GRCh37.p13 chr7: 128,332,168-128,332,563 IMP3P2, GARIN1A
    nsv6822042copy number variation1nstd229human GRCh38 chr7: 128,690,701-128,697,400 , GRCh37.p13 chr7: 128,330,755-128,337,454 RNA5SP242, RNA5SP243, 2 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6434966copy number variation1nstd223human GRCh38 chr7: 128,663,683-128,676,302 , GRCh37.p13 chr7: 128,303,737-128,316,356 GARIN1A
    nsv6419193copy number variation1nstd223human GRCh38 chr7: 128,700,775-128,701,457 , GRCh37.p13 chr7: 128,340,829-128,341,511 GARIN1A
    nsv6416468copy number variation1nstd223human GRCh38 chr7: 128,688,601-128,690,300 , GRCh37.p13 chr7: 128,328,655-128,330,354 GARIN1A
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
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