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Items: 1 to 20 of 109

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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
    nsv7095260copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,940,783-10,941,723 , GRCh38.p12 chr19: 10,830,107-10,831,047 TMED1, DNM2
    nsv7064560inversion1nstd229human GRCh38 chr19: 10,835,810-10,841,429 , GRCh37.p13 chr19: 10,946,486-10,952,105 C19orf38, TMED1
    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
    nsv7060620inversion1nstd229human GRCh38 chr19: 10,833,371-10,841,782 , GRCh37.p13 chr19: 10,944,047-10,952,458 TMED1, C19orf38
    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
    nsv7010368copy number variation1nstd229human GRCh38 chr19: 10,831,938-10,832,092 , GRCh37.p13 chr19: 10,942,614-10,942,768 DNM2, TMED1
    nsv7007297copy number variation1nstd229human GRCh38 chr19: 10,836,505-10,838,311 , GRCh37.p13 chr19: 10,947,181-10,948,987 TMED1, C19orf38
    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
    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
    nsv6637648copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,871,121-11,012,295 , GRCh38.p12 chr19: 10,760,445-10,901,619 TMED1, DNM2, 5 more genes
    nsv6596677inversion1nstd223human GRCh38 chr19: 10,733,096-10,849,613 , GRCh37.p13 chr19: 10,843,772-10,960,289 DNM2, TMED1, 4 more genes
    nsv6519481copy number variation1nstd223human GRCh38 chr19: 10,825,263-10,844,576 , GRCh37.p13 chr19: 10,935,939-10,955,252 C19orf38, TMED1, 2 more genes
    nsv6310437copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,939,692-10,941,723 , GRCh38.p12 chr19: 10,829,016-10,831,047 TMED1, MIR6793, 1 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
    nsv5517513copy number variation1nstd206human GRCh38 chr19: 10,832,065-10,832,319 , GRCh37.p13 chr19: 10,942,741-10,942,995 TMED1, DNM2
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