U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 249

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7017345copy number variation1nstd229human GRCh38 chr19: 36,654,235-36,658,714 , GRCh37.p13 chr19: 37,145,137-37,149,616 ZNF461
    nsv7009562copy number variation1nstd229human GRCh38 chr19: 36,643,901-36,668,300 , GRCh37.p13 chr19: 37,134,803-37,159,202 ZNF461, ZNF567
    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
    nsv7002379copy number variation1nstd229human GRCh38 chr19: 36,644,160-36,645,679 , GRCh37.p13 chr19: 37,135,062-37,136,581 ZNF461
    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
    nsv6600031inversion1nstd223human GRCh38 chr19: 36,644,864-36,645,120 , GRCh37.p13 chr19: 37,135,766-37,136,022 ZNF461
    nsv6597372inversion1nstd223human GRCh38 chr19: 36,322,830-37,322,723 , GRCh37.p13 chr19: 36,813,732-37,813,625 ZNF790, RPL31P61, 28 more genes
    nsv6597248inversion1nstd223human GRCh38 chr19: 36,646,131-36,647,539 , GRCh37.p13 chr19: 37,137,033-37,138,441 ZNF461
    nsv6596160inversion1nstd223human GRCh38 chr19: 36,649,625-36,649,929 , GRCh37.p13 chr19: 37,140,527-37,140,831 ZNF461
    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
    nsv6522799copy number variation1nstd223human GRCh38 chr19: 36,644,157-36,645,675 , GRCh37.p13 chr19: 37,135,059-37,136,577 ZNF461
    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
    nsv6251026mobile element insertion1nstd215human GRCh38 chr19: 36,665,215-36,665,215 , GRCh37.p13 chr19: 37,156,117-37,156,117 ZNF461, ZNF567
    nsv6251025mobile element insertion1nstd215human GRCh38 chr19: 36,663,941-36,663,941 , GRCh37.p13 chr19: 37,154,843-37,154,843 ZNF461
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5936864copy number variation1nstd209human GRCh38 chr19: 36,649,391-36,667,714 , GRCh37.p13 chr19: 37,140,293-37,158,616 ZNF567, ZNF461
    nsv5883846copy number variation1nstd209human GRCh38 chr19: 36,652,497-36,653,796 , GRCh37.p13 chr19: 37,143,399-37,144,698 ZNF461
    nsv5873271copy number variation1nstd209human GRCh38 chr19: 36,652,686-36,667,561 , GRCh37.p13 chr19: 37,143,588-37,158,463 ZNF461, ZNF567
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center