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Items: 1 to 20 of 225

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7017249copy number variation1nstd229human GRCh38 chr19: 36,612,869-36,613,663 , GRCh37.p13 chr19: 37,103,771-37,104,565 ZNF382
    nsv7013410copy number variation1nstd229human GRCh38 chr19: 36,616,879-36,617,006 , GRCh37.p13 chr19: 37,107,781-37,107,908 ZNF382
    nsv7012218copy number variation1nstd229human GRCh38 chr19: 36,608,155-36,611,727 , GRCh37.p13 chr19: 37,099,057-37,102,629 ZNF382
    nsv7010672copy number variation1nstd229human GRCh38 chr19: 36,610,902-36,614,415 , GRCh37.p13 chr19: 37,101,804-37,105,317 ZNF382
    nsv7005843copy number variation1nstd229human GRCh38 chr19: 36,614,662-36,617,761 , GRCh37.p13 chr19: 37,105,564-37,108,663 ZNF382
    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
    nsv6624889copy number variation1nstd224human GRCh37 chr19: 37,047,472-37,238,758 , GRCh38.p12 chr19: 36,556,570-36,747,856 ZNF529, ZNF382, 5 more genes
    nsv6599719inversion1nstd223human GRCh38 chr19: 36,613,089-36,614,214 , GRCh37.p13 chr19: 37,103,991-37,105,116 ZNF382
    nsv6598726inversion1nstd223human GRCh38 chr19: 36,606,487-36,607,045 , GRCh37.p13 chr19: 37,097,389-37,097,947 ZNF382
    nsv6597372inversion1nstd223human GRCh38 chr19: 36,322,830-37,322,723 , GRCh37.p13 chr19: 36,813,732-37,813,625 ZNF790, RPL31P61, 28 more genes
    nsv6535180copy number variation1nstd223human GRCh38 chr19: 36,416,491-37,213,522 , GRCh37.p13 chr19: 36,907,393-37,704,424 LOC644189, ZNF566-AS1, 22 more genes
    nsv6531235copy number variation1nstd223human GRCh38 chr19: 36,610,902-36,614,412 , GRCh37.p13 chr19: 37,101,804-37,105,314 ZNF382
    nsv6524880copy number variation1nstd223human GRCh38 chr19: 36,612,944-36,613,704 , GRCh37.p13 chr19: 37,103,846-37,104,606 ZNF382
    nsv6520792copy number variation1nstd223human GRCh38 chr19: 36,610,627-36,661,034 , GRCh37.p13 chr19: 37,101,529-37,151,936 ZNF461, ZNF382
    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
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5942622copy number variation1nstd209human GRCh38 chr19: 36,616,879-36,617,005 , GRCh37.p13 chr19: 37,107,781-37,107,907 ZNF382
    nsv5702204mobile element insertion1nstd211human GRCh38 chr19: 36,621,346-36,621,346 , GRCh37.p13 chr19: 37,112,248-37,112,248 ZNF382
    nsv5531446copy number variation1nstd206human GRCh38 chr19: 36,629,204-36,725,597 , GRCh37.p13 chr19: 37,120,106-37,216,499 ZNF461, ZNF567-DT, 2 more genes
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