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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7074279inversion1nstd229human GRCh38 chr19: 33,135,428-36,017,833 , GRCh37.p13 chr19: 33,626,334-36,508,735 , PSENEN, 122 more genes
    nsv7012206copy number variation1nstd229human GRCh38 chr19: 35,833,783-36,008,471 , GRCh37.p13 chr19: 36,324,685-36,499,373 TYROBP, SYNE4, 11 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7005456copy number variation1nstd229human GRCh38 chr19: 35,863,391-36,727,332 , GRCh37.p13 chr19: 36,354,293-37,218,234 ZNF146, CLIP3, 39 more genes
    nsv6532655copy number variation1nstd223human GRCh38 chr19: 35,818,262-36,019,433 , GRCh37.p13 chr19: 36,309,164-36,510,335 TYROBP, LOC101927572, 13 more genes
    nsv6530021copy number variation1nstd223human GRCh38 chr19: 36,007,849-36,020,429 , GRCh37.p13 chr19: 36,498,751-36,511,331 CLIP3, LOC101927572, 2 more genes
    nsv6310629copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,521,725-36,643,309 , GRCh38.p12 chr19: 35,030,821-36,152,407 KRTDAP, WDR62, 78 more genes
    nsv6291710copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,019,064-36,516,110 , GRCh38.p12 chr19: 35,528,162-36,025,208 NFKBID, APLP1, 38 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133701copy number variation1nstd213human GRCh37 chr19: 36,490,000-36,640,001 , GRCh38.p12 chr19: 35,999,098-36,149,099 CAPNS1, TBCB, 11 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5289021copy number variation1nstd204human GRCh38.p13 chr19: 36,002,801-36,145,200 , GRCh37.p13 chr19: 36,493,703-36,636,102 LOC101927572, THAP8, 10 more genes
    nsv5024579copy number variation1nstd200human GRCh38 chr19: 36,005,869-36,025,618 , GRCh37.p13 chr19: 36,496,771-36,516,520 LOC101927572, ALKBH6, 2 more genes
    nsv5024572copy number variation1nstd200human GRCh38 chr19: 35,818,267-36,019,433 , GRCh37.p13 chr19: 36,309,169-36,510,335 SYNE4, LOC107985317, 13 more genes
    nsv5024570copy number variation1nstd200human GRCh38 chr19: 35,722,805-36,225,611 , GRCh37.p13 chr19: 36,213,707-36,716,513 LOC105372385, ALKBH6, 34 more genes
    nsv4865133copy number variation1nstd200human GRCh37 chr19: 36,213,707-36,716,513 , GRCh38.p12 chr19: 35,722,805-36,225,611 KMT2B, PSENEN, 34 more genes
    nsv4625448copy number variation1nstd183human GRCh37 chr19: 36,505,480-36,505,524 , GRCh38.p12 chr19: 36,014,578-36,014,622 CLIP3, ALKBH6, 1 more genes
    nsv4536962copy number variation1nstd166human GRCh37.p13 chr19: 36,309,999-36,510,300 , GRCh38.p12 chr19: 35,819,097-36,019,398 KIRREL2, HCST, 13 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
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