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Items: 1 to 20 of 518

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7017013copy number variation1nstd229human GRCh38 chr19: 36,370,446-36,412,548 , GRCh37.p13 chr19: 36,861,348-36,903,450 ZFP14, ZFP82
    nsv7010397copy number variation1nstd229human GRCh38 chr19: 36,349,851-36,356,173 , GRCh37.p13 chr19: 36,840,753-36,847,075 ZFP14
    nsv7009029copy number variation1nstd229human GRCh38 chr19: 36,343,834-36,354,186 , GRCh37.p13 chr19: 36,834,736-36,845,088 ZFP14
    nsv7007593copy number variation1nstd229human GRCh38 chr19: 36,342,101-36,343,400 , GRCh37.p13 chr19: 36,833,003-36,834,302 ZFP14
    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
    nsv7005043copy number variation1nstd229human GRCh38 chr19: 36,329,536-36,335,593 , GRCh37.p13 chr19: 36,820,438-36,826,495 LINC00665, ZFP14
    nsv6998518copy number variation1nstd229human GRCh38 chr19: 36,341,401-36,378,100 , GRCh37.p13 chr19: 36,832,303-36,869,002 ZFP14
    nsv6599680inversion1nstd223human GRCh38 chr19: 36,344,147-36,345,271 , GRCh37.p13 chr19: 36,835,049-36,836,173 ZFP14
    nsv6597372inversion1nstd223human GRCh38 chr19: 36,322,830-37,322,723 , GRCh37.p13 chr19: 36,813,732-37,813,625 ZNF790, RPL31P61, 28 more genes
    nsv6597272inversion1nstd223human GRCh38 chr19: 36,363,373-36,363,708 , GRCh37.p13 chr19: 36,854,275-36,854,610 ZFP14
    nsv6595778inversion1nstd223human GRCh38 chr19: 36,356,305-36,357,075 , GRCh37.p13 chr19: 36,847,207-36,847,977 ZFP14
    nsv6534918copy number variation1nstd223human GRCh38 chr19: 36,330,301-36,488,900 , GRCh37.p13 chr19: 36,821,203-36,979,802 ZFP14, LOC644189, 4 more genes
    nsv6533650copy number variation1nstd223human GRCh38 chr19: 36,333,594-36,335,022 , GRCh37.p13 chr19: 36,824,496-36,825,924 ZFP14
    nsv6521137copy number variation1nstd223human GRCh38 chr19: 36,351,950-36,352,563 , GRCh37.p13 chr19: 36,842,852-36,843,465 ZFP14
    nsv6517849copy number variation1nstd223human GRCh38 chr19: 36,348,401-36,356,200 , GRCh37.p13 chr19: 36,839,303-36,847,102 ZFP14
    nsv6515720copy number variation1nstd223human GRCh38 chr19: 36,373,016-36,374,229 , GRCh37.p13 chr19: 36,863,918-36,865,131 ZFP14
    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
    nsv6251023mobile element insertion1nstd215human GRCh38 chr19: 36,359,386-36,359,386 , GRCh37.p13 chr19: 36,850,288-36,850,288 ZFP14
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
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