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Items: 1 to 20 of 947

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139840insertion1nstd232human GRCh37.p13 chr10: 21,346,518-21,346,518 , GRCh38.p12 chr10: 21,057,589-21,057,589 NEBL
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7074105inversion1nstd229human GRCh38 chr10: 17,945,641-22,801,235 , GRCh37.p13 chr10: 18,252,931-23,090,164 UBE2V2P1, LOC105376450, 62 more genes
    nsv7070711inversion1nstd229human GRCh38 chr10: 20,788,452-20,800,245 , GRCh37.p13 chr10: 21,077,381-21,089,174 NEBL
    nsv7070090inversion1nstd229human GRCh38 chr10: 21,223,003-21,310,174 , GRCh37.p13 chr10: 21,511,932-21,599,103 NEBL
    nsv7066925inversion1nstd229human GRCh38 chr10: 20,923,340-20,925,988 , GRCh37.p13 chr10: 21,212,269-21,214,917 NEBL
    nsv7066222inversion1nstd229human GRCh38 chr10: 21,281,529-21,304,654 , GRCh37.p13 chr10: 21,570,458-21,593,583 NEBL
    nsv7061268inversion1nstd229human GRCh38 chr10: 20,901,307-20,904,338 , GRCh37.p13 chr10: 21,190,236-21,193,267 NEBL
    nsv7060918inversion1nstd229human GRCh38 chr10: 21,291,002-21,306,305 , GRCh37.p13 chr10: 21,579,931-21,595,234 NEBL
    nsv7060528inversion1nstd229human GRCh38 chr10: 21,106,863-21,110,976 , GRCh37.p13 chr10: 21,395,792-21,399,905 NEBL, NPM1P30
    nsv6897968copy number variation1nstd229human GRCh38 chr10: 21,201,488-21,206,031 , GRCh37.p13 chr10: 21,490,417-21,494,960 NEBL
    nsv6897610copy number variation1nstd229human GRCh38 chr10: 20,837,099-20,843,497 , GRCh37.p13 chr10: 21,126,028-21,132,426 NEBL, LOC102725112
    nsv6897431copy number variation1nstd229human GRCh38 chr10: 20,950,397-20,954,773 , GRCh37.p13 chr10: 21,239,326-21,243,702 NEBL
    nsv6897384copy number variation1nstd229human GRCh38 chr10: 21,185,350-21,200,755 , GRCh37.p13 chr10: 21,474,279-21,489,684 NEBL
    nsv6897305copy number variation1nstd229human GRCh38 chr10: 21,220,005-21,241,621 , GRCh37.p13 chr10: 21,508,934-21,530,550 NEBL
    nsv6897253copy number variation1nstd229human GRCh38 chr10: 20,967,567-20,983,428 , GRCh37.p13 chr10: 21,256,496-21,272,357 NEBL
    nsv6897155copy number variation1nstd229human GRCh38 chr10: 21,282,381-21,302,563 , GRCh37.p13 chr10: 21,571,310-21,591,492 NEBL
    nsv6897019copy number variation1nstd229human GRCh38 chr10: 20,810,395-20,812,260 , GRCh37.p13 chr10: 21,099,324-21,101,189 NEBL
    nsv6896354copy number variation1nstd229human GRCh38 chr10: 20,763,438-20,783,781 , GRCh37.p13 chr10: 21,052,367-21,072,710 NEBL
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