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Items: 1 to 20 of 127

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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
    nsv7014220copy number variation1nstd229human GRCh38 chr19: 36,111,339-36,111,428 , GRCh37.p13 chr19: 36,602,241-36,602,330 WDR62, OVOL3
    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
    nsv7000686copy number variation1nstd229human GRCh38 chr19: 36,094,511-36,127,632 , GRCh37.p13 chr19: 36,585,413-36,618,534 POLR2I, LOC105372385, 3 more genes
    nsv6999792copy number variation1nstd229human GRCh38 chr19: 36,044,743-36,166,690 , GRCh37.p13 chr19: 36,535,645-36,657,592 LOC105372385, COX7A1, 8 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
    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
    nsv6145633copy number variation1nstd206human GRCh38 chr19: 36,104,874-36,110,874 , GRCh37.p13 chr19: 36,595,776-36,601,776 OVOL3, WDR62
    nsv6145427copy number variation1nstd206human GRCh38 chr19: 36,016,874-36,114,874 , GRCh37.p13 chr19: 36,507,776-36,605,776 TBCB, POLR2I, 6 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
    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
    nsv4680891copy number variation1nstd189human GRCh37.p13 chr19: 36,586,154-37,723,606 , GRCh38.p12 chr19: 36,095,252-37,232,704 CAPNS1, TBCB, 36 more genes
    nsv4631779copy number variation1nstd183human GRCh37 chr19: 36,604,763-36,604,909 , GRCh38.p12 chr19: 36,113,861-36,114,007 TBCB, OVOL3, 1 more genes
    nsv4457836copy number variation1nstd102humanUncertain significance GRCh37 chr19: 36,570,287-36,655,341 , GRCh38.p12 chr19: 36,079,385-36,164,439 OVOL3, TBCB, 5 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
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
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