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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965041insertion1nstd209human GRCh38 chr9: 2,821,443-2,821,443 , GRCh37.p13 chr9: 2,821,443-2,821,443 PUM3
    nsv5706161mobile element insertion1nstd211human GRCh38 chr9: 2,815,348-2,815,348 , GRCh37.p13 chr9: 2,815,348-2,815,348 PUM3
    nsv5694837mobile element insertion1nstd211human GRCh38 chr9: 2,814,154-2,814,154 , GRCh37.p13 chr9: 2,814,154-2,814,154 PUM3
    nsv5643877insertion1nstd207human GRCh38 chr9: 2,814,057-2,814,057 , GRCh37.p13 chr9: 2,814,057-2,814,057 PUM3
    nsv5486857copy number variation1nstd206human GRCh38 chr9: 2,814,057-2,814,259 , GRCh37.p13 chr9: 2,814,057-2,814,259 PUM3
    nsv5405569mobile element insertion1nstd206human GRCh38 chr9: 2,815,348-2,815,399 , GRCh37.p13 chr9: 2,815,348-2,815,399 PUM3
    nsv5387294copy number variation2nstd186human GRCh37 chr9: 2,814,057-2,814,259 , GRCh38.p12 chr9: 2,814,057-2,814,259 PUM3
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 ACTG1P14, DMAC1, 191 more genes
    nsv5381702copy number variation1nstd102humanUncertain significance GRCh37 chr9: 2,029,023-5,300,444 , GRCh38.p12 chr9: 2,029,023-5,300,444 MTND5P36, MTND2P36, 53 more genes
    nsv5372208translocation1nstd200human GRCh38 chr9: 2,847,203-2,847,203 , GRCh38 chr9: 2,844,291-2,844,291 , GRCh37.p13 chr9: 2,844,291-2,844,291 , GRCh37.p13 chr9: 2,847,203-2,847,203 PUM3
    nsv5308587copy number variation1nstd204human GRCh38.p13 chr9: 2,814,057-2,814,259 , GRCh37.p13 chr9: 2,814,057-2,814,259 PUM3
    nsv5186127mobile element insertion1nstd203human GRCh38 chr9: 2,813,288-2,813,306 , GRCh37.p13 chr9: 2,813,288-2,813,306 PUM3
    nsv4969261copy number variation1nstd200human GRCh38 chr9: 2,826,144-2,868,906 , GRCh37.p13 chr9: 2,826,144-2,868,906 PUM3
    nsv4969260copy number variation1nstd200human GRCh38 chr9: 2,814,057-2,814,259 , GRCh37.p13 chr9: 2,814,057-2,814,259 PUM3
    nsv4962964copy number variation1nstd200human GRCh38 chr9: 2,840,221-2,849,282 , GRCh37.p13 chr9: 2,840,221-2,849,282 PUM3
    nsv4962963copy number variation1nstd200human GRCh38 chr9: 2,839,260-2,846,539 , GRCh37.p13 chr9: 2,839,260-2,846,539 PUM3
    nsv4962962copy number variation1nstd200human GRCh38 chr9: 2,832,183-2,832,434 , GRCh37.p13 chr9: 2,832,183-2,832,434 PUM3
    nsv4962955copy number variation1nstd200human GRCh38 chr9: 2,716,899-2,855,266 , GRCh37.p13 chr9: 2,716,899-2,855,266 PUM3, KCNV2
    nsv4962953copy number variation1nstd200human GRCh38 chr9: 2,695,020-2,825,626 , GRCh37.p13 chr9: 2,695,020-2,825,626 KCNV2, PUM3
    nsv4823047copy number variation1nstd200human GRCh37 chr9: 2,695,020-2,825,626 , GRCh38.p12 chr9: 2,695,020-2,825,626 PUM3, KCNV2
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