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 203

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7059793inversion1nstd229human GRCh38 chr19: 36,784,643-37,649,443 , GRCh37.p13 chr19: 37,275,545-38,140,344 ZNF790-AS1, ZNF829, 24 more genes
    nsv7013628copy number variation1nstd229human GRCh38 chr19: 36,945,425-37,379,636 , GRCh37.p13 chr19: 37,436,327-37,870,538 ZNF585B, ZNF875, 8 more genes
    nsv7009961copy number variation1nstd229human GRCh38 chr19: 37,380,786-37,387,616 , GRCh37.p13 chr19: 37,871,688-37,878,518 ZNF527
    nsv7009513copy number variation1nstd229human GRCh38 chr19: 37,378,979-37,379,161 , GRCh37.p13 chr19: 37,869,881-37,870,063 ZNF527
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7004813copy number variation1nstd229human GRCh38 chr19: 37,384,019-37,391,695 , GRCh37.p13 chr19: 37,874,921-37,882,597 ZNF527
    nsv7001094copy number variation1nstd229human GRCh38 chr19: 37,363,982-37,385,410 , GRCh37.p13 chr19: 37,854,884-37,876,312 ZNF875, ZNF527
    nsv6637740copy number variation1nstd102humanUncertain significance GRCh37 chr19: 37,389,799-38,562,489 , GRCh38.p12 chr19: 36,898,897-38,071,849 MTND5P45, ZNF568, 36 more genes
    nsv6624866copy number variation1nstd224human GRCh37 chr19: 37,835,641-37,917,692 , GRCh38.p12 chr19: 37,344,739-37,426,790 ZNF527, ZNF875, 1 more genes
    nsv6624711copy number variation1nstd224human GRCh37 chr19: 37,613,594-37,988,445 , GRCh38.p12 chr19: 37,122,692-37,497,543 ZNF527, ZNF585B, 9 more genes
    nsv6624465copy number variation1nstd224human GRCh37 chr19: 37,797,578-37,894,468 , GRCh38.p12 chr19: 37,306,676-37,403,566 ZNF527, ZNF875
    nsv6596929inversion1nstd223human GRCh38 chr19: 37,383,855-37,384,029 , GRCh37.p13 chr19: 37,874,757-37,874,931 ZNF527
    nsv6596399inversion1nstd223human GRCh38 chr19: 37,383,839-37,384,116 , GRCh37.p13 chr19: 37,874,741-37,875,018 ZNF527
    nsv6595627inversion1nstd223human GRCh38 chr19: 37,383,559-37,384,317 , GRCh37.p13 chr19: 37,874,461-37,875,219 ZNF527
    nsv6528926copy number variation1nstd223human GRCh38 chr19: 37,386,447-37,388,006 , GRCh37.p13 chr19: 37,877,349-37,878,908 ZNF527
    nsv6518621copy number variation1nstd223human GRCh38 chr19: 37,363,982-37,385,410 , GRCh37.p13 chr19: 37,854,884-37,876,312 ZNF875, ZNF527
    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
    nsv5698447mobile element insertion1nstd211human GRCh38 chr19: 37,380,643-37,380,643 , GRCh37.p13 chr19: 37,871,545-37,871,545 ZNF527
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

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