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 109

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071846inversion1nstd229human GRCh38 chr19: 57,519,061-57,653,276 , GRCh37.p13 chr19: 58,030,429-58,164,644 ZNF134, ZNF416, 6 more genes
    nsv7071416inversion1nstd229human GRCh38 chr19: 57,448,527-57,827,280 , GRCh37.p13 chr19: 57,959,895-58,338,648 VN1R1, ZSCAN4, 19 more genes
    nsv7013959copy number variation1nstd229human GRCh38 chr19: 57,560,883-57,682,885 , GRCh37.p13 chr19: 58,072,251-58,194,253 ZNF530, ZNF550, 7 more genes
    nsv6999110copy number variation1nstd229human GRCh38 chr19: 57,288,372-57,890,926 , GRCh37.p13 chr19: 57,799,740-58,402,294 ZNF460, ZNF551, 32 more genes
    nsv6597711inversion1nstd223human GRCh38 chr19: 55,930,883-58,410,519 , GRCh37.p13 chr19: 56,442,249-58,921,886 ZNF667-AS1, ZNF606-AS1, 130 more genes
    nsv6597167inversion1nstd223human GRCh38 chr19: 55,930,699-58,410,630 , GRCh37.p13 chr19: 56,442,065-58,921,997 VN2R19P, RPL19P19, 130 more genes
    nsv6291743copy number variation1nstd102humanLikely benign GRCh37 chr19: 58,026,985-58,255,427 , GRCh38.p12 chr19: 57,515,617-57,744,059 ZSCAN4, ZNF671, 11 more genes
    nsv6133477copy number variation1nstd213human GRCh37 chr19: 57,800,000-59,128,983 , GRCh38.p12 chr19: 57,288,632-58,607,616 A1BG, FKBP1AP1, 95 more genes
    nsv6133413copy number variation1nstd213human GRCh37 chr19: 57,870,000-59,128,983 , GRCh38.p12 chr19: 57,358,632-58,607,616 ZNF8, ZNF211, 92 more genes
    nsv5644593insertion1nstd207human GRCh38 chr19: 57,612,821-57,612,821 , GRCh37.p13 chr19: 58,124,189-58,124,189 ZNF134, ZNF530
    nsv5380327translocation1nstd200human GRCh38 chrX: 117,497,478-117,497,478 , GRCh38 chr19: 57,600,536-57,600,536 , GRCh37.p13 chrX: 116,631,441-116,631,441 , GRCh37.p13 chr19: 58,111,904-58,111,904 ZNF530
    nsv5340971translocation1nstd200human GRCh37 chr19: 58,111,904-58,111,904 , GRCh37 chrX: 116,631,441-116,631,441 , GRCh38.p12 chr19: 57,600,536-57,600,536 , GRCh38.p12 chrX: 117,497,478-117,497,478 ZNF530
    nsv5300321copy number variation1nstd204human GRCh38.p13 chr19: 57,611,939-57,641,301 , GRCh37.p13 chr19: 58,123,307-58,152,669 ZNF530, ZNF134, 1 more genes
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv5288591copy number variation1nstd204human GRCh38.p13 chr19: 57,577,805-57,603,361 , GRCh37.p13 chr19: 58,089,173-58,114,729 ZIK1, ZNF530, 1 more genes
    nsv5280624copy number variation1nstd204human GRCh38.p13 chr19: 57,527,801-57,913,300 , GRCh37.p13 chr19: 58,039,169-58,424,668 ZNF549, ZNF417, 19 more genes
    nsv4457732copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,952,073-58,661,581 , GRCh38.p12 chr19: 57,440,705-58,150,214 ZNF418, ZNF606-AS1, 39 more genes
    nsv4457626copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,092,045-58,686,148 , GRCh38.p12 chr19: 57,580,677-58,174,781 ZNF417, ZSCAN1, 30 more genes
    nsv4457535copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,054,819-58,410,552 , GRCh38.p12 chr19: 57,543,451-57,899,184 ZNF587B, ZNF530, 17 more genes
    nsv4264516copy number variation1nstd166human GRCh37.p13 chr19: 58,012,736-58,148,044 , GRCh38.p12 chr19: 57,501,368-57,636,676 ZNF134, ZNF211, 6 more genes
    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