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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138638insertion1nstd232human GRCh37.p13 chr19: 10,273,424-10,273,424 , GRCh38.p12 chr19: 10,162,748-10,162,748 DNMT1
    nsv7138113insertion1nstd232human GRCh37.p13 chr19: 10,251,007-10,251,007 , GRCh38.p12 chr19: 10,140,331-10,140,331 DNMT1
    nsv7095457copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,244,343-10,245,003 , GRCh38.p12 chr19: 10,133,667-10,134,327 DNMT1
    nsv7095259copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,244,343-10,251,024 , GRCh38.p12 chr19: 10,133,667-10,140,348 DNMT1
    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
    nsv7012863copy number variation1nstd229human GRCh38 chr19: 10,148,854-10,156,030 , GRCh37.p13 chr19: 10,259,530-10,266,706 DNMT1
    nsv7000466copy number variation1nstd229human GRCh38 chr19: 10,184,165-10,187,787 , GRCh37.p13 chr19: 10,294,841-10,298,463 DNMT1
    nsv6999748copy number variation1nstd229human GRCh38 chr19: 10,102,367-10,133,810 , GRCh37.p13 chr19: 10,213,043-10,244,486 EIF3G, SNORD105, 6 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
    nsv6598873inversion1nstd223human GRCh38 chr19: 10,160,879-10,162,142 , GRCh37.p13 chr19: 10,271,555-10,272,818 DNMT1
    nsv6598051inversion1nstd223human GRCh38 chr19: 10,160,887-10,161,994 , GRCh37.p13 chr19: 10,271,563-10,272,670 DNMT1
    nsv6528510copy number variation1nstd223human GRCh38 chr19: 10,102,367-10,133,807 , GRCh37.p13 chr19: 10,213,043-10,244,483 PPAN, ANGPTL6, 6 more genes
    nsv6526269copy number variation1nstd223human GRCh38 chr19: 10,148,004-10,148,384 , GRCh37.p13 chr19: 10,258,680-10,259,060 DNMT1
    nsv6522120copy number variation1nstd223human GRCh38 chr19: 10,170,372-10,171,539 , GRCh37.p13 chr19: 10,281,048-10,282,215 DNMT1
    nsv6518596copy number variation1nstd223human GRCh38 chr19: 10,147,852-10,148,235 , GRCh37.p13 chr19: 10,258,528-10,258,911 DNMT1
    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
    nsv6205305copy number variation1nstd214human GRCh38 chr19: 10,182,415-10,182,484 , GRCh37.p13 chr19: 10,293,091-10,293,160 DNMT1
    nsv6205255copy number variation1nstd214human GRCh38 chr19: 10,182,454-10,182,513 , GRCh37.p13 chr19: 10,293,130-10,293,189 DNMT1
    nsv6201453copy number variation1nstd214human GRCh38 chr19: 10,182,442-10,182,515 , GRCh37.p13 chr19: 10,293,118-10,293,191 DNMT1
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