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Items: 1 to 20 of 792

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148204copy number variation1nstd102humanPathogenic GRCh38 chr5: 9,999-14,320,000 , GRCh37.p13 chr5: 10,001-14,320,109 LOC105379638, LOC100420683, 185 more genes
    nsv7053901inversion1nstd229human GRCh38 chr5: 3,129,013-8,027,353 , GRCh37.p13 chr5: 3,129,127-8,027,466 FASTKD3, LOC101929200, 58 more genes
    nsv7045426inversion1nstd229human GRCh38 chr5: 3,060,043-5,252,130 , GRCh37.p13 chr5: 3,060,157-5,252,243 LOC107986400, LINC02063, 16 more genes
    nsv7045223inversion1nstd229human GRCh38 chr5: 2,721,510-7,652,208 , GRCh37.p13 chr5: 2,721,624-7,652,321 LOC105374620, LOC105374634, 60 more genes
    nsv7042270inversion1nstd229human GRCh38 chr5: 4,344,295-6,275,858 , GRCh37.p13 chr5: 4,344,408-6,275,971 LOC105374629, MTCO2P30, 15 more genes
    nsv7040546inversion1nstd229human GRCh38 chr5: 4,326,347-6,141,150 , GRCh37.p13 chr5: 4,326,460-6,141,263 LOC105374634, MTCO1P31, 15 more genes
    nsv6777564copy number variation1nstd229human GRCh38 chr5: 5,155,850-5,165,920 , GRCh37.p13 chr5: 5,155,963-5,166,033 ADAMTS16
    nsv6777294copy number variation1nstd229human GRCh38 chr5: 5,211,469-5,361,374 , GRCh37.p13 chr5: 5,211,582-5,361,487 LOC101929200, ADAMTS16
    nsv6776616copy number variation1nstd229human GRCh38 chr5: 5,156,531-5,170,026 , GRCh37.p13 chr5: 5,156,644-5,170,139 ADAMTS16
    nsv6775751copy number variation1nstd229human GRCh38 chr5: 5,191,011-5,191,077 , GRCh37.p13 chr5: 5,191,124-5,191,190 ADAMTS16
    nsv6775316copy number variation1nstd229human GRCh38 chr5: 5,211,874-5,219,866 , GRCh37.p13 chr5: 5,211,987-5,219,979 ADAMTS16
    nsv6774749copy number variation1nstd229human GRCh38 chr5: 5,244,501-5,249,400 , GRCh37.p13 chr5: 5,244,614-5,249,513 ADAMTS16
    nsv6774652copy number variation1nstd229human GRCh38 chr5: 4,946,640-6,484,597 , GRCh37.p13 chr5: 4,946,753-6,484,710 RN7SKP73, LINC01020, 17 more genes
    nsv6773778copy number variation1nstd229human GRCh38 chr5: 5,147,228-5,157,437 , GRCh37.p13 chr5: 5,147,341-5,157,550 ADAMTS16
    nsv6771074copy number variation1nstd229human GRCh38 chr5: 5,148,501-5,151,000 , GRCh37.p13 chr5: 5,148,614-5,151,113 ADAMTS16
    nsv6770203copy number variation1nstd229human GRCh38 chr5: 5,171,828-5,179,630 , GRCh37.p13 chr5: 5,171,941-5,179,743 ADAMTS16
    nsv6768670copy number variation1nstd229human GRCh38 chr5: 5,303,322-5,312,611 , GRCh37.p13 chr5: 5,303,435-5,312,724 LOC101929200, ADAMTS16
    nsv6766669copy number variation1nstd229human GRCh38 chr5: 5,260,085-5,262,221 , GRCh37.p13 chr5: 5,260,198-5,262,334 ADAMTS16, LOC101929200
    nsv6765294copy number variation1nstd229human GRCh38 chr5: 5,195,396-5,195,509 , GRCh37.p13 chr5: 5,195,509-5,195,622 ADAMTS16
    nsv6765199copy number variation1nstd229human GRCh38 chr5: 5,093,729-5,718,574 , GRCh37.p13 chr5: 5,093,842-5,718,687 MTCO1P30, ADAMTS16, 8 more genes
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