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Items: 1 to 20 of 379

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140117insertion1nstd232human GRCh37.p13 chr19: 10,869,019-10,869,019 , GRCh38.p12 chr19: 10,758,343-10,758,343 DNM2
    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
    nsv7095260copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,940,783-10,941,723 , GRCh38.p12 chr19: 10,830,107-10,831,047 TMED1, DNM2
    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
    nsv7015858copy number variation1nstd229human GRCh38 chr19: 10,728,957-10,736,278 , GRCh37.p13 chr19: 10,839,633-10,846,954 DNM2
    nsv7013931copy number variation1nstd229human GRCh38 chr19: 10,794,301-10,934,700 , GRCh37.p13 chr19: 10,904,977-11,045,376 DNM2, CARM1, 6 more genes
    nsv7012417copy number variation1nstd229human GRCh38 chr19: 10,751,564-10,753,238 , GRCh37.p13 chr19: 10,862,240-10,863,914 DNM2
    nsv7011942copy number variation1nstd229human GRCh38 chr19: 10,790,851-10,792,646 , GRCh37.p13 chr19: 10,901,527-10,903,322 DNM2
    nsv7010429copy number variation1nstd229human GRCh38 chr19: 10,767,981-10,768,339 , GRCh37.p13 chr19: 10,878,657-10,879,015 DNM2
    nsv7010368copy number variation1nstd229human GRCh38 chr19: 10,831,938-10,832,092 , GRCh37.p13 chr19: 10,942,614-10,942,768 DNM2, TMED1
    nsv7010309copy number variation1nstd229human GRCh38 chr19: 10,761,211-10,763,235 , GRCh37.p13 chr19: 10,871,887-10,873,911 DNM2
    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
    nsv7005410copy number variation1nstd229human GRCh38 chr19: 10,761,041-10,763,235 , GRCh37.p13 chr19: 10,871,717-10,873,911 DNM2
    nsv7005125copy number variation1nstd229human GRCh38 chr19: 10,829,001-10,833,300 , GRCh37.p13 chr19: 10,939,677-10,943,976 DNM2, MIR6793, 1 more genes
    nsv7002366copy number variation1nstd229human GRCh38 chr19: 10,772,450-10,772,724 , GRCh37.p13 chr19: 10,883,126-10,883,400 DNM2
    nsv7001861copy number variation1nstd229human GRCh38 chr19: 10,814,001-10,816,964 , GRCh37.p13 chr19: 10,924,677-10,927,640 DNM2, MIR199A1
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