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Items: 1 to 20 of 362

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7071620inversion1nstd229human GRCh38 chr10: 71,272,229-71,275,010 , GRCh37.p13 chr10: 73,031,986-73,034,767 UNC5B
    nsv7061181inversion1nstd229human GRCh38 chr10: 71,284,421-71,284,510 , GRCh37.p13 chr10: 73,044,178-73,044,267 UNC5B
    nsv7058306inversion1nstd229human GRCh38 chr10: 71,209,770-71,317,966 , GRCh37.p13 chr10: 72,969,527-73,077,723 SLC29A3, LOC112268061, 2 more genes
    nsv6897657copy number variation1nstd229human GRCh38 chr10: 71,288,245-71,625,893 , GRCh37.p13 chr10: 73,048,002-73,385,650 LOC105378353, UNC5B, 5 more genes
    nsv6897453copy number variation1nstd229human GRCh38 chr10: 71,269,701-71,307,900 , GRCh37.p13 chr10: 73,029,458-73,067,657 UNC5B
    nsv6891775copy number variation1nstd229human GRCh38 chr10: 71,303,200-71,306,241 , GRCh37.p13 chr10: 73,062,957-73,065,998 UNC5B
    nsv6891101copy number variation1nstd229human GRCh38 chr10: 71,228,203-71,232,663 , GRCh37.p13 chr10: 72,987,960-72,992,420 UNC5B
    nsv6890930copy number variation1nstd229human GRCh38 chr10: 71,174,318-71,658,626 , GRCh37.p13 chr10: 72,934,075-73,418,383 UNC5B, CDH23-AS1, 7 more genes
    nsv6890879copy number variation1nstd229human GRCh38 chr10: 71,302,500-71,302,593 , GRCh37.p13 chr10: 73,062,257-73,062,350 UNC5B
    nsv6890397copy number variation1nstd229human GRCh38 chr10: 71,218,101-71,223,600 , GRCh37.p13 chr10: 72,977,858-72,983,357 UNC5B, UNC5B-AS1
    nsv6888685copy number variation1nstd229human GRCh38 chr10: 71,215,461-71,216,856 , GRCh37.p13 chr10: 72,975,218-72,976,613 UNC5B-AS1, UNC5B
    nsv6888399copy number variation1nstd229human GRCh38 chr10: 71,230,991-71,233,545 , GRCh37.p13 chr10: 72,990,748-72,993,302 UNC5B
    nsv6888167copy number variation1nstd229human GRCh38 chr10: 71,296,712-71,296,762 , GRCh37.p13 chr10: 73,056,469-73,056,519 UNC5B
    nsv6887400copy number variation1nstd229human GRCh38 chr10: 71,297,702-71,306,294 , GRCh37.p13 chr10: 73,057,459-73,066,051 UNC5B
    nsv6885973copy number variation1nstd229human GRCh38 chr10: 71,219,131-71,222,252 , GRCh37.p13 chr10: 72,978,888-72,982,009 UNC5B
    nsv6885148copy number variation1nstd229human GRCh38 chr10: 71,200,599-71,272,906 , GRCh37.p13 chr10: 72,960,356-73,032,663 UNC5B-AS1, UNC5B, 1 more genes
    nsv6884970copy number variation1nstd229human GRCh38 chr10: 71,207,301-71,219,800 , GRCh37.p13 chr10: 72,967,058-72,979,557 UNC5B, UNC5B-AS1
    nsv6884561copy number variation1nstd229human GRCh38 chr10: 71,197,245-71,475,767 , GRCh37.p13 chr10: 72,957,002-73,235,524 CDH23, LOC112268061, 5 more genes
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