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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6597866inversion1nstd223human GRCh38 chr19: 57,662,682-57,663,462 , GRCh37.p13 chr19: 58,174,050-58,174,830 TPRG1LP1, ZSCAN4
    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
    nsv6596127inversion1nstd223human GRCh38 chr19: 57,661,910-57,662,630 , GRCh37.p13 chr19: 58,173,278-58,173,998 TPRG1LP1, ZSCAN4
    nsv6535492copy number variation1nstd223human GRCh38 chr19: 57,662,149-57,967,273 , GRCh37.p13 chr19: 58,173,517-58,478,641 ZNF587B, ZNF552, 16 more genes
    nsv6529426copy number variation1nstd223human GRCh38 chr19: 57,663,193-57,716,324 , GRCh37.p13 chr19: 58,174,561-58,227,692 TPRG1LP1, ZNF551, 2 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
    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
    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
    nsv5025013copy number variation1nstd200human GRCh38 chr19: 57,662,149-57,967,273 , GRCh37.p13 chr19: 58,173,517-58,478,641 ZNF814, C19orf18, 16 more genes
    nsv4631981copy number variation1nstd183human GRCh37 chr19: 58,167,451-58,210,489 , GRCh38.p12 chr19: 57,656,083-57,699,121 ZNF154, ZNF551, 2 more genes
    nsv4506926mobile element insertion1nstd166human GRCh37.p13 chr19: 58,174,710-58,174,710 , GRCh38.p12 chr19: 57,663,342-57,663,342 TPRG1LP1, ZSCAN4
    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
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