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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7095400copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,277,234-13,249,220 , GRCh38.p12 chr19: 11,166,558-13,138,406 ZNF627, RGL3, 120 more genes
    nsv7065930inversion1nstd229human GRCh38 chr19: 12,331,349-12,331,517 , GRCh37.p13 chr19: 12,442,163-12,442,331 ZNF563
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7058761inversion1nstd229human GRCh38 chr19: 12,041,264-12,373,051 , GRCh37.p13 chr19: 12,152,079-12,483,865 RPS2P53, ZNF625-ZNF20, 17 more genes
    nsv7013321copy number variation1nstd229human GRCh38 chr19: 12,336,531-12,345,858 , GRCh37.p13 chr19: 12,447,345-12,456,672 ZNF442, ZNF563
    nsv7010261copy number variation1nstd229human GRCh38 chr19: 12,346,101-12,349,200 , GRCh37.p13 chr19: 12,456,915-12,460,014 ZNF442, ZNF563
    nsv7003548copy number variation1nstd229human GRCh38 chr19: 12,343,726-12,347,488 , GRCh37.p13 chr19: 12,454,540-12,458,302 ZNF442, ZNF563
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6598460inversion1nstd223human GRCh38 chr19: 12,329,207-12,330,106 , GRCh37.p13 chr19: 12,440,021-12,440,920 ZNF563
    nsv6598381inversion1nstd223human GRCh38 chr19: 12,316,077-12,317,593 , GRCh37.p13 chr19: 12,426,891-12,428,407 ZNF563
    nsv6598075inversion1nstd223human GRCh38 chr19: 12,338,881-12,339,310 , GRCh37.p13 chr19: 12,449,695-12,450,124 ZNF563
    nsv6147022sequence alteration1nstd206human GRCh38 chr19: 12,342,928-12,343,067 , GRCh37.p13 chr19: 12,453,742-12,453,881 ZNF563
    nsv6133689copy number variation1nstd213human GRCh37 chr19: 11,220,000-13,700,001 , GRCh38.p12 chr19: 11,109,324-13,589,187 ACP5, GET3, 128 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5932082copy number variation1nstd209human GRCh38 chr19: 12,336,518-12,345,843 , GRCh37.p13 chr19: 12,447,332-12,456,657 ZNF442, ZNF563
    nsv5521022copy number variation1nstd206human GRCh38 chr19: 12,333,560-12,333,627 , GRCh37.p13 chr19: 12,444,374-12,444,441 ZNF563
    nsv5161554mobile element insertion1nstd203human GRCh38 chr19: 12,342,779-12,342,779 , GRCh37.p13 chr19: 12,453,593-12,453,593 ZNF563
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