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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5533226copy number variation1nstd206human GRCh38 chr20: 68,334-3,826,335 , GRCh37.p13 chr20: 60,002-3,806,982 , SNORD110, 125 more genes
    nsv5521914copy number variation1nstd206human GRCh38 chr20: 3,196,550-3,197,775 , GRCh37.p13 chr20: 3,177,196-3,178,421 DDRGK1
    nsv5327925copy number variation1nstd204human GRCh38.p13 chr20: 3,196,235-3,197,380 , GRCh37.p13 chr20: 3,176,881-3,178,026 DDRGK1
    nsv5179908mobile element insertion1nstd203human GRCh38 chr20: 3,196,503-3,196,513 , GRCh37.p13 chr20: 3,177,149-3,177,159 DDRGK1
    nsv5178708mobile element insertion1nstd203human GRCh38 chr20: 3,196,531-3,196,555 , GRCh37.p13 chr20: 3,177,177-3,177,201 DDRGK1
    nsv5170969mobile element insertion1nstd203human GRCh38 chr20: 3,196,513-3,196,531 , GRCh37.p13 chr20: 3,177,159-3,177,177 DDRGK1
    nsv5166502mobile element insertion1nstd203human GRCh38 chr20: 3,196,521-3,196,531 , GRCh37.p13 chr20: 3,177,167-3,177,177 DDRGK1
    nsv5012203copy number variation1nstd200human GRCh38 chr20: 3,196,448-3,198,125 , GRCh37.p13 chr20: 3,177,094-3,178,771 DDRGK1
    nsv4865414copy number variation1nstd200human GRCh37 chr20: 3,177,148-3,177,813 , GRCh38.p12 chr20: 3,196,502-3,197,167 DDRGK1
    nsv4861686copy number variation1nstd200human GRCh37 chr20: 3,177,155-3,178,380 , GRCh38.p12 chr20: 3,196,509-3,197,734 DDRGK1
    nsv4729952copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,116,478-4,199,486 , GRCh38.p12 chr20: 3,135,832-4,218,839 LOC105372508, CDC25B, 35 more genes
    nsv4729947copy number variation1nstd102humanUncertain significance GRCh37 chr20: 3,092,739-4,939,933 , GRCh38.p12 chr20: 3,112,093-4,959,287 SF3A3P1, PRND, 46 more genes
    nsv4729753copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,802,218-4,010,802 , GRCh38.p12 chr20: 2,821,572-4,030,155 DDRGK1, LZTS3, 40 more genes
    nsv4676134copy number variation1nstd102humanUncertain significance GRCh37 chr20: 2,806,498-4,007,381 , GRCh38.p12 chr20: 2,825,852-4,026,734 MIR103B2, OXT, 40 more genes
    nsv4626453copy number variation1nstd183human GRCh37 chr20: 3,020,553-3,350,814 , GRCh38.p12 chr20: 3,039,907-3,370,167 DDRGK1, FASTKD5, 16 more genes
    nsv4417768copy number variation1nstd174human GRCh37 chr20: 3,011,188-3,385,073 , GRCh38.p12 chr20: 3,030,542-3,404,426 LZTS3, UBOX5, 17 more genes
    nsv4349190copy number variation1nstd102humanPathogenic GRCh37 chr20: 61,568-26,305,479 , GRCh38.p12 chr20: 80,927-26,324,843 LOC105372582, LOC101929937, 473 more genes
    nsv4330625inversion1nstd166human GRCh37.p13 chr20: 2,496,151-5,491,306 , GRCh38.p12 chr20: 2,515,505-5,510,660 , ADRA1D, 89 more genes
    nsv4262351copy number variation1nstd166human GRCh37.p13 chr20: 3,180,093-3,181,054 , GRCh38.p12 chr20: 3,199,447-3,200,408 DDRGK1
    nsv4254125copy number variation1nstd166human GRCh37.p13 chr20: 3,182,254-3,182,356 , GRCh38.p12 chr20: 3,201,608-3,201,710 DDRGK1
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