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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976704inversion1nstd209human GRCh38 chr20: 36,955,252-45,585,469 , GRCh37.p13 chr20: 35,583,655-44,214,108 , ADA, 180 more genes
    nsv5975125insertion1nstd209human GRCh38 chr20: 38,020,320-38,020,320 , GRCh37.p13 chr20: 36,648,722-36,648,722 TTI1
    nsv5962394copy number variation1nstd209human GRCh38 chr20: 38,027,301-38,028,405 , GRCh37.p13 chr20: 36,655,703-36,656,807 TTI1
    nsv5961061copy number variation1nstd209human GRCh38 chr20: 37,997,456-37,998,516 , GRCh37.p13 chr20: 36,625,858-36,626,918 TTI1
    nsv5878154copy number variation1nstd209human GRCh38 chr20: 37,997,418-37,998,540 , GRCh37.p13 chr20: 36,625,820-36,626,942 TTI1
    nsv5520063copy number variation1nstd206human GRCh38 chr20: 37,997,459-37,998,517 , GRCh37.p13 chr20: 36,625,861-36,626,919 TTI1
    nsv5350329translocation1nstd200human GRCh38 chr20: 37,998,517-37,998,517 , GRCh38 chr20: 37,997,459-37,997,459 , GRCh37.p13 chr20: 36,625,861-36,625,861 , GRCh37.p13 chr20: 36,626,919-36,626,919 TTI1
    nsv5330770translocation1nstd200human GRCh37 chr20: 36,626,919-36,626,919 , GRCh37 chr20: 36,625,861-36,625,861 , GRCh38.p12 chr20: 37,998,517-37,998,517 , GRCh38.p12 chr20: 37,997,459-37,997,459 TTI1
    nsv5327445copy number variation1nstd204human GRCh38.p13 chr20: 37,997,458-37,998,517 , GRCh37.p13 chr20: 36,625,860-36,626,919 TTI1
    nsv5324090inversion1nstd204human GRCh37.p13 chr20: 35,583,652-44,214,109 , GRCh38.p13 chr20: 36,955,249-45,585,470 , BPI, 180 more genes
    nsv5289297copy number variation1nstd204human GRCh38.p13 chr20: 37,997,418-37,998,940 , GRCh37.p13 chr20: 36,625,820-36,627,342 TTI1
    nsv5285926copy number variation1nstd204human GRCh38.p13 chr20: 37,997,501-37,998,500 , GRCh37.p13 chr20: 36,625,903-36,626,902 TTI1
    nsv5168846mobile element insertion1nstd203human GRCh38 chr20: 38,031,169-38,031,185 , GRCh37.p13 chr20: 36,659,571-36,659,587 TTI1
    nsv5033948inversion1nstd200human GRCh38 chr20: 36,955,253-45,585,464 , GRCh37.p13 chr20: 35,583,656-44,214,103 , EMILIN3, 180 more genes
    nsv5025577copy number variation1nstd200human GRCh38 chr20: 37,996,399-38,000,531 , GRCh37.p13 chr20: 36,624,801-36,628,933 TTI1
    nsv5022343copy number variation1nstd200human GRCh38 chr20: 32,602,560-45,347,064 , GRCh37.p13 chr20: 31,190,362-43,975,704 , SNHG11, 286 more genes
    nsv5022342copy number variation1nstd200human GRCh38 chr20: 32,576,247-46,538,786 , GRCh37.p13 chr20: 31,164,049-45,167,425 , NECAB3, 350 more genes
    nsv5022326copy number variation1nstd200human GRCh38 chr20: 32,216,214-44,981,731 , GRCh37.p13 chr20: 30,804,017-43,610,372 , HNF4A, 279 more genes
    nsv4884257inversion1nstd200human GRCh37 chr20: 35,583,656-44,214,103 , GRCh38.p12 chr20: 36,955,253-45,585,464 , TGM2, 180 more genes
    nsv4868593copy number variation1nstd200human GRCh37 chr20: 31,164,049-45,167,425 , GRCh38.p12 chr20: 32,576,247-46,538,786 , MMP24-AS1-EDEM2, 350 more genes
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