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Items: 1 to 20 of 781

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129029insertion1nstd186human GRCh37 chrX: 69,054,933-69,054,984 , GRCh38.p12 chrX: 69,835,089-69,835,140 EDA
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5978780copy number variation1nstd209human GRCh38 chrX: 69,751,660-69,758,868 , GRCh37.p13 chrX: 68,971,504-68,978,712 EDA
    nsv5976665copy number variation1nstd209human GRCh38 chrX: 69,802,649-69,806,448 , GRCh37.p13 chrX: 69,022,493-69,026,292 EDA
    nsv5976160inversion1nstd209human GRCh38 chrX: 68,979,629-71,845,571 , GRCh37.p13 chrX: 68,199,472-71,065,421 ARR3, DLG3, 73 more genes
    nsv5948467insertion1nstd209human GRCh38 chrX: 69,645,594-69,645,594 , GRCh37.p13 chrX: 68,865,438-68,865,438 EDA
    nsv5886420copy number variation1nstd209human GRCh38 chrX: 69,751,197-69,759,028 , GRCh37.p13 chrX: 68,971,041-68,978,872 EDA
    nsv5881468copy number variation1nstd209human GRCh38 chrX: 70,019,500-70,019,552 , GRCh37.p13 chrX: 69,239,350-69,239,402 EDA
    nsv5880944copy number variation1nstd209human GRCh38 chrX: 69,980,741-69,981,528 , GRCh37.p13 chrX: 69,200,591-69,201,378 EDA
    nsv5880738copy number variation1nstd209human GRCh38 chrX: 69,751,799-78,490,154 , GRCh37.p13 chrX: 68,971,643-77,745,651 , MTND4P31, 183 more genes
    nsv5878497copy number variation1nstd209human GRCh38 chrX: 69,751,829-69,751,886 , GRCh37.p13 chrX: 68,971,673-68,971,730 EDA
    nsv5876520copy number variation1nstd209human GRCh38 chrX: 69,764,991-69,765,082 , GRCh37.p13 chrX: 68,984,835-68,984,926 EDA
    nsv5872618copy number variation1nstd209human GRCh38 chrX: 69,803,194-69,806,401 , GRCh37.p13 chrX: 69,023,038-69,026,245 EDA
    nsv5727922mobile element insertion2nstd211human GRCh38 chrX: 69,685,533-69,685,533 , GRCh37.p13 chrX: 68,905,377-68,905,377 EDA
    nsv5727396mobile element insertion1nstd211human GRCh38 chrX: 69,997,796-69,997,796 , GRCh37.p13 chrX: 69,217,646-69,217,646 EDA
    nsv5722969mobile element insertion1nstd211human GRCh38 chrX: 69,749,949-69,749,949 , GRCh37.p13 chrX: 68,969,793-68,969,793 EDA
    nsv5722124mobile element insertion1nstd211human GRCh38 chrX: 69,845,586-69,845,586 , GRCh37.p13 chrX: 69,065,426-69,065,426 EDA
    nsv5720868mobile element insertion2nstd211human GRCh38 chrX: 69,641,565-69,641,565 , GRCh37.p13 chrX: 68,861,409-68,861,409 EDA
    nsv5673902copy number variation1nstd102humanPathogenic GRCh37 chrX: 69,247,757-69,247,869 , GRCh38 chrX: 70,027,907-70,028,019 EDA
    nsv5673839copy number variation1nstd102humanPathogenic GRCh37 chrX: 69,247,786-69,247,871 , GRCh38 chrX: 70,027,936-70,028,021 EDA
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