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Items: 1 to 20 of 459

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061788inversion1nstd229human GRCh38 chr19: 36,446,875-36,542,222 , GRCh37.p13 chr19: 36,937,777-37,033,124 ZNF529, CTBP2P7, 3 more genes
    nsv7017499copy number variation1nstd229human GRCh38 chr19: 36,521,505-36,535,836 , GRCh37.p13 chr19: 37,012,407-37,026,738 ZNF529, ZNF260
    nsv7014518copy number variation1nstd229human GRCh38 chr19: 36,554,078-36,572,036 , GRCh37.p13 chr19: 37,044,980-37,062,938 ZNF529-AS1, ZNF529
    nsv7012824copy number variation1nstd229human GRCh38 chr19: 36,563,185-36,566,784 , GRCh37.p13 chr19: 37,054,087-37,057,686 ZNF529
    nsv7012181copy number variation1nstd229human GRCh38 chr19: 36,555,293-36,555,595 , GRCh37.p13 chr19: 37,046,195-37,046,497 ZNF529
    nsv7011169copy number variation1nstd229human GRCh38 chr19: 36,567,913-36,576,068 , GRCh37.p13 chr19: 37,058,815-37,066,970 ZNF529, ZNF529-AS1
    nsv7008535copy number variation1nstd229human GRCh38 chr19: 36,529,342-36,533,680 , GRCh37.p13 chr19: 37,020,244-37,024,582 ZNF529
    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
    nsv7004607copy number variation1nstd229human GRCh38 chr19: 36,529,877-36,553,428 , GRCh37.p13 chr19: 37,020,779-37,044,330 ZNF529
    nsv7002206copy number variation1nstd229human GRCh38 chr19: 36,584,344-36,591,459 , GRCh37.p13 chr19: 37,075,246-37,082,361 ZNF529-AS1, ZNF529
    nsv6999610copy number variation1nstd229human GRCh38 chr19: 36,540,019-36,549,530 , GRCh37.p13 chr19: 37,030,921-37,040,432 ZNF529
    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
    nsv6598376inversion1nstd223human GRCh38 chr19: 36,575,946-36,576,721 , GRCh37.p13 chr19: 37,066,848-37,067,623 ZNF529, ZNF529-AS1
    nsv6597410inversion1nstd223human GRCh38 chr19: 36,578,673-36,579,066 , GRCh37.p13 chr19: 37,069,575-37,069,968 ZNF529, ZNF529-AS1
    nsv6597372inversion1nstd223human GRCh38 chr19: 36,322,830-37,322,723 , GRCh37.p13 chr19: 36,813,732-37,813,625 ZNF790, RPL31P61, 28 more genes
    nsv6595687inversion1nstd223human GRCh38 chr19: 36,532,237-36,533,217 , GRCh37.p13 chr19: 37,023,139-37,024,119 ZNF529
    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
    nsv6532349copy number variation1nstd223human GRCh38 chr19: 36,547,093-36,547,679 , GRCh37.p13 chr19: 37,037,995-37,038,581 ZNF529
    nsv6528755copy number variation1nstd223human GRCh38 chr19: 36,530,533-36,567,561 , GRCh37.p13 chr19: 37,021,435-37,058,463 ZNF529
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