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Items: 1 to 20 of 155

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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
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7063283inversion1nstd229human GRCh38 chr19: 11,910,405-12,006,197 , GRCh37.p13 chr19: 12,021,220-12,117,012 VN2R21P, VN2R15P, 6 more genes
    nsv7061164inversion1nstd229human GRCh38 chr19: 11,962,059-11,967,051 , GRCh37.p13 chr19: 12,072,874-12,077,866 ZNF763, ZNF69
    nsv7017126copy number variation1nstd229human GRCh38 chr19: 11,961,689-12,018,515 , GRCh37.p13 chr19: 12,072,504-12,129,330 ZNF69, ZNF433-AS1, 3 more genes
    nsv7015659copy number variation1nstd229human GRCh38 chr19: 11,824,251-12,016,223 , GRCh37.p13 chr19: 11,935,066-12,127,038 VN2R21P, VN2R14P, 11 more genes
    nsv7012691copy number variation1nstd229human GRCh38 chr19: 11,979,951-11,984,939 , GRCh37.p13 chr19: 12,090,766-12,095,754 ZNF69, ZNF763
    nsv7012647copy number variation1nstd229human GRCh38 chr19: 11,977,201-11,979,400 , GRCh37.p13 chr19: 12,088,016-12,090,215 ZNF763, ZNF69
    nsv7006493copy number variation1nstd229human GRCh38 chr19: 11,935,764-12,004,858 , GRCh37.p13 chr19: 12,046,579-12,115,673 ZNF69, ZNF700, 4 more genes
    nsv6999294copy number variation1nstd229human GRCh38 chr19: 11,836,894-12,128,680 , GRCh37.p13 chr19: 11,947,709-12,239,495 ZNF700, VN2R21P, 17 more genes
    nsv6637950copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,753,820-12,272,905 , GRCh38.p12 chr19: 11,643,005-12,162,090 ZNF433, ZNF878, 29 more genes
    nsv6599518inversion1nstd223human GRCh38 chr19: 11,975,380-11,978,339 , GRCh37.p13 chr19: 12,086,195-12,089,154 ZNF763, ZNF69
    nsv6598443inversion1nstd223human GRCh38 chr19: 11,975,534-11,976,547 , GRCh37.p13 chr19: 12,086,349-12,087,362 ZNF69, ZNF763
    nsv6598229inversion1nstd223human GRCh38 chr19: 11,967,280-11,967,541 , GRCh37.p13 chr19: 12,078,095-12,078,356 ZNF69, ZNF763
    nsv6596228inversion1nstd223human GRCh38 chr19: 11,975,156-11,976,419 , GRCh37.p13 chr19: 12,085,971-12,087,234 ZNF69, ZNF763
    nsv6291774copy number variation1nstd102humanUncertain significance GRCh37 chr19: 12,061,304-12,242,460 , GRCh38.p12 chr19: 11,950,489-12,131,645 ZNF69, VN2R21P, 14 more genes
    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
    nsv6129847insertion1nstd186human GRCh37 chr19: 12,073,904-12,073,954 , GRCh38.p12 chr19: 11,963,089-11,963,139 ZNF69, ZNF763
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