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Items: 1 to 20 of 98

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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
    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
    nsv7095179copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,828,919-10,829,099 , GRCh38.p12 chr19: 10,718,243-10,718,423 MIR638, DNM2
    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
    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
    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
    nsv5564401copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,828,909-10,829,089 , GRCh38.p12 chr19: 10,718,233-10,718,413 MIR638, DNM2
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4682991copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,828,909-10,870,497 , GRCh38.p12 chr19: 10,718,233-10,759,821 DNM2, MIR638
    nsv4682378copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,828,909-10,897,392 , GRCh38.p12 chr19: 10,718,233-10,786,716 DNM2, MIR4748, 1 more genes
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 ATG4D, RN7SL192P, 21 more genes
    nsv4628771copy number variation1nstd183human GRCh37 chr19: 10,788,813-10,988,086 , GRCh38.p12 chr19: 10,678,137-10,877,410 DNM2, CARM1, 8 more genes
    nsv4624289copy number variation1nstd183human GRCh37 chr19: 10,828,540-10,829,040 , GRCh38.p12 chr19: 10,717,864-10,718,364 MIR638, DNM2
    nsv4457721copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,441,330-10,977,962 , GRCh38.p12 chr19: 10,330,654-10,867,286 CDKN2D, QTRT1, 24 more genes
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