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Items: 1 to 20 of 243

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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
    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
    nsv7015253copy number variation1nstd229human GRCh38 chr19: 10,621,868-10,624,247 , GRCh37.p13 chr19: 10,732,544-10,734,923 SLC44A2
    nsv7014850copy number variation1nstd229human GRCh38 chr19: 10,637,747-10,637,854 , GRCh37.p13 chr19: 10,748,423-10,748,530 SLC44A2
    nsv7013213copy number variation1nstd229human GRCh38 chr19: 10,616,479-10,627,101 , GRCh37.p13 chr19: 10,727,155-10,737,777 SLC44A2
    nsv7005260copy number variation1nstd229human GRCh38 chr19: 10,639,582-10,639,775 , GRCh37.p13 chr19: 10,750,258-10,750,451 SLC44A2
    nsv7003626copy number variation1nstd229human GRCh38 chr19: 10,632,157-10,634,754 , GRCh37.p13 chr19: 10,742,833-10,745,430 SLC44A2
    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
    nsv6598897inversion1nstd223human GRCh38 chr19: 10,606,192-10,607,082 , GRCh37.p13 chr19: 10,716,868-10,717,758 SLC44A2
    nsv6532291copy number variation1nstd223human GRCh38 chr19: 10,622,557-10,644,661 , GRCh37.p13 chr19: 10,733,233-10,755,337 SLC44A2
    nsv6530215copy number variation1nstd223human GRCh38 chr19: 10,606,895-10,607,809 , GRCh37.p13 chr19: 10,717,571-10,718,485 SLC44A2
    nsv6527815copy number variation1nstd223human GRCh38 chr19: 10,632,835-10,633,298 , GRCh37.p13 chr19: 10,743,511-10,743,974 SLC44A2
    nsv6523038copy number variation1nstd223human GRCh38 chr19: 10,602,101-10,602,700 , GRCh37.p13 chr19: 10,712,777-10,713,376 SLC44A2
    nsv6518782copy number variation1nstd223human GRCh38 chr19: 10,634,110-10,661,613 , GRCh37.p13 chr19: 10,744,786-10,772,289 ILF3, SLC44A2, 1 more genes
    nsv6518778copy number variation1nstd223human GRCh38 chr19: 10,608,706-10,609,878 , GRCh37.p13 chr19: 10,719,382-10,720,554 SLC44A2
    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
    nsv6206506copy number variation1nstd214human GRCh38 chr19: 10,611,510-10,611,560 , GRCh37.p13 chr19: 10,722,186-10,722,236 SLC44A2
    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
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