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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098944copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,624,491-10,969,019 , GRCh38.p12 chr19: 10,513,815-10,858,343 DNM2, ILF3-DT, 17 more genes
    nsv7072297inversion1nstd229human GRCh38 chr19: 10,695,423-10,825,346 , GRCh37.p13 chr19: 10,806,099-10,936,022 QTRT1, DNM2, 3 more genes
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv7014652copy number variation1nstd229human GRCh38 chr19: 10,705,806-10,710,586 , GRCh37.p13 chr19: 10,816,482-10,821,262 QTRT1
    nsv7008486copy number variation1nstd229human GRCh38 chr19: 10,656,482-10,749,047 , GRCh37.p13 chr19: 10,767,158-10,859,723 MIR638, QTRT1, 2 more genes
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6599940inversion1nstd223human GRCh38 chr19: 10,699,152-10,700,386 , GRCh37.p13 chr19: 10,809,828-10,811,062 QTRT1
    nsv6596945inversion1nstd223human GRCh38 chr19: 10,710,435-10,710,749 , GRCh37.p13 chr19: 10,821,111-10,821,425 QTRT1
    nsv6532361copy number variation1nstd223human GRCh38 chr19: 10,703,636-10,711,423 , GRCh37.p13 chr19: 10,814,312-10,822,099 QTRT1
    nsv6528304copy number variation1nstd223human GRCh38 chr19: 10,705,816-10,710,557 , GRCh37.p13 chr19: 10,816,492-10,821,233 QTRT1
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 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
    nsv6102919insertion1nstd212human GRCh38 chr19: 10,699,496-10,699,496 , GRCh37.p13 chr19: 10,810,172-10,810,172 QTRT1
    nsv5975987insertion1nstd209human GRCh38 chr19: 10,709,693-10,709,693 , GRCh37.p13 chr19: 10,820,369-10,820,369 QTRT1
    nsv5932266copy number variation1nstd209human GRCh38 chr19: 10,707,162-10,707,348 , GRCh37.p13 chr19: 10,817,838-10,818,024 QTRT1
    nsv5728830mobile element insertion1nstd211human GRCh38 chr19: 10,705,870-10,705,870 , GRCh37.p13 chr19: 10,816,546-10,816,546 QTRT1
    nsv5720529mobile element insertion1nstd211human GRCh38 chr19: 10,705,642-10,705,642 , GRCh37.p13 chr19: 10,816,318-10,816,318 QTRT1
    nsv5532185copy number variation1nstd206human GRCh38 chr19: 10,707,339-10,707,427 , GRCh37.p13 chr19: 10,818,015-10,818,103 QTRT1
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