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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5897894copy number variation1nstd209human GRCh38 chr6: 43,643,741-43,643,795 , GRCh37.p13 chr6: 43,611,478-43,611,532 RSPH9
    nsv5890731copy number variation1nstd209human GRCh38 chr6: 43,647,109-43,647,173 , GRCh37.p13 chr6: 43,614,846-43,614,910 RSPH9
    nsv5673766copy number variation1nstd102humanPathogenic GRCh37 chr6: 42,928,506-43,737,486 , GRCh38.p12 chr6: 42,960,768-43,769,749 SRF, POLR1C, 39 more genes
    nsv5567296copy number variation1nstd207human GRCh38 chr6: 43,647,109-43,647,173 , GRCh37.p13 chr6: 43,614,846-43,614,910 RSPH9
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5459751copy number variation1nstd206human GRCh38 chr6: 43,662,511-43,663,322 , GRCh37.p13 chr6: 43,630,248-43,631,059 RSPH9
    nsv5454889copy number variation1nstd206human GRCh38 chr6: 43,647,112-43,647,174 , GRCh37.p13 chr6: 43,614,849-43,614,911 RSPH9
    nsv5454294copy number variation1nstd206human GRCh38 chr6: 43,643,741-43,643,797 , GRCh37.p13 chr6: 43,611,478-43,611,534 RSPH9
    nsv5362903translocation1nstd200human GRCh38 chr6: 43,647,112-43,647,112 , GRCh38 chr6: 43,647,174-43,647,174 , GRCh37.p13 chr6: 43,614,911-43,614,911 , GRCh37.p13 chr6: 43,614,849-43,614,849 RSPH9
    nsv5334645translocation1nstd200human GRCh37 chr6: 43,611,478-43,611,478 , GRCh37 chr6: 43,611,534-43,611,534 , GRCh38.p12 chr6: 43,643,741-43,643,741 , GRCh38.p12 chr6: 43,643,797-43,643,797 RSPH9
    nsv5226309copy number variation1nstd204human GRCh38.p13 chr6: 43,660,619-43,661,618 , GRCh37.p13 chr6: 43,628,356-43,629,355 RSPH9
    nsv5117096mobile element insertion1nstd203human GRCh38 chr6: 43,651,961-43,651,982 , GRCh37.p13 chr6: 43,619,698-43,619,719 RSPH9
    nsv5103754mobile element insertion1nstd203human GRCh38 chr6: 43,646,595-43,646,611 , GRCh37.p13 chr6: 43,614,332-43,614,348 RSPH9
    nsv4941157copy number variation1nstd200human GRCh38 chr6: 43,658,834-43,658,944 , GRCh37.p13 chr6: 43,626,571-43,626,681 RSPH9
    nsv4941156copy number variation1nstd200human GRCh38 chr6: 43,643,741-43,643,798 , GRCh37.p13 chr6: 43,611,478-43,611,535 RSPH9
    nsv4934686copy number variation1nstd200human GRCh38 chr6: 43,660,485-43,664,368 , GRCh37.p13 chr6: 43,628,222-43,632,105 RSPH9
    nsv4816209copy number variation1nstd200human GRCh37 chr6: 43,627,233-43,630,207 , GRCh38.p12 chr6: 43,659,496-43,662,470 RSPH9
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4756329inversion1nstd199human GRCh37 chr6: 26,745,246-58,149,317 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
    nsv4735754copy number variation1nstd199human GRCh37 chr6: 26,776,020-58,144,810 , GRCh38.p12 chr6: 26,823,536-61,119,912 , RNU6-250P, 1075 more genes
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