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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131344insertion1nstd186human GRCh37 chr19: 10,293,797-10,293,801 , GRCh38.p12 chr19: 10,183,121-10,183,125 DNMT1
    nsv5940804copy number variation1nstd209human GRCh38 chr19: 10,182,367-10,182,424 , GRCh37.p13 chr19: 10,293,043-10,293,100 DNMT1
    nsv5928723copy number variation1nstd209human GRCh38 chr19: 10,151,240-10,151,320 , GRCh37.p13 chr19: 10,261,916-10,261,996 DNMT1
    nsv5881972copy number variation1nstd209human GRCh38 chr19: 10,175,994-10,177,293 , GRCh37.p13 chr19: 10,286,670-10,287,969 DNMT1
    nsv5598979copy number variation1nstd207human GRCh38 chr19: 10,182,391-10,182,462 , GRCh37.p13 chr19: 10,293,067-10,293,138 DNMT1
    nsv5534461insertion1nstd206human GRCh38 chr19: 10,183,121-10,183,125 , GRCh37.p13 chr19: 10,293,797-10,293,801 DNMT1
    nsv5531316copy number variation1nstd206human GRCh38 chr19: 10,178,662-10,179,037 , GRCh37.p13 chr19: 10,289,338-10,289,713 DNMT1
    nsv5529708copy number variation1nstd206human GRCh38 chr19: 10,151,243-10,151,321 , GRCh37.p13 chr19: 10,261,919-10,261,997 DNMT1
    nsv5527082copy number variation1nstd206human GRCh38 chr19: 10,147,832-10,148,255 , GRCh37.p13 chr19: 10,258,508-10,258,931 DNMT1
    nsv5521688copy number variation1nstd206human GRCh38 chr19: 10,180,636-10,180,715 , GRCh37.p13 chr19: 10,291,312-10,291,391 DNMT1
    nsv5521493copy number variation1nstd206human GRCh38 chr19: 10,171,633-10,172,211 , GRCh37.p13 chr19: 10,282,309-10,282,887 DNMT1
    nsv5516799copy number variation1nstd206human GRCh38 chr19: 10,187,556-10,187,823 , GRCh37.p13 chr19: 10,298,232-10,298,499 DNMT1
    nsv5359473translocation1nstd200human GRCh38 chr19: 10,161,530-10,161,530 , GRCh38 chr19: 10,161,427-10,161,427 , GRCh37.p13 chr19: 10,272,103-10,272,103 , GRCh37.p13 chr19: 10,272,206-10,272,206 DNMT1
    nsv5328193copy number variation1nstd204human GRCh38.p13 chr19: 10,179,738-10,189,935 , GRCh37.p13 chr19: 10,290,414-10,300,611 DNMT1
    nsv5298537copy number variation1nstd204human GRCh38.p13 chr19: 10,179,630-10,184,805 , GRCh37.p13 chr19: 10,290,306-10,295,481 DNMT1
    nsv5291057copy number variation1nstd204human GRCh38.p13 chr19: 10,179,701-10,189,900 , GRCh37.p13 chr19: 10,290,377-10,300,576 DNMT1
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5208799mobile element deletion1nstd204human GRCh38.p13 chr19: 10,162,291-10,162,562 , GRCh37.p13 chr19: 10,272,967-10,273,238 DNMT1
    nsv5179484mobile element insertion1nstd203human GRCh38 chr19: 10,152,160-10,152,200 , GRCh37.p13 chr19: 10,262,836-10,262,876 DNMT1
    nsv5177526mobile element insertion1nstd203human GRCh38 chr19: 10,171,812-10,171,830 , GRCh37.p13 chr19: 10,282,488-10,282,506 DNMT1
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