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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7048454inversion1nstd229human GRCh38 chr7: 80,780,894-80,843,002 , GRCh37.p13 chr7: 80,410,210-80,472,318 SEMA3C
    nsv7048114inversion1nstd229human GRCh38 chr7: 76,979,006-85,395,330 , GRCh37.p13 chr7: 76,608,323-85,024,646 LOC100420647, LOC105375369, 77 more genes
    nsv7039908inversion1nstd229human GRCh38 chr7: 80,783,795-80,783,847 , GRCh37.p13 chr7: 80,413,111-80,413,163 SEMA3C
    nsv7038572inversion1nstd229human GRCh38 chr7: 79,747,222-82,700,267 , GRCh37.p13 chr7: 79,376,538-82,329,583 CACNA2D1-AS1, SNRPBP1, 25 more genes
    nsv6836712copy number variation1nstd229human GRCh38 chr7: 80,892,976-80,894,676 , GRCh37.p13 chr7: 80,522,292-80,523,992 SEMA3C
    nsv6836532copy number variation1nstd229human GRCh38 chr7: 80,784,461-80,926,574 , GRCh37.p13 chr7: 80,413,777-80,555,890 SEMA3C
    nsv6834394copy number variation1nstd229human GRCh38 chr7: 80,837,043-80,837,625 , GRCh37.p13 chr7: 80,466,359-80,466,941 SEMA3C
    nsv6834062copy number variation1nstd229human GRCh38 chr7: 80,371,260-81,570,787 , GRCh37.p13 chr7: 80,000,576-81,200,103 EIF4EP4, LOC101927269, 7 more genes
    nsv6833300copy number variation1nstd229human GRCh38 chr7: 80,858,503-80,858,703 , GRCh37.p13 chr7: 80,487,819-80,488,019 SEMA3C
    nsv6830817copy number variation1nstd229human GRCh38 chr7: 80,893,253-80,898,564 , GRCh37.p13 chr7: 80,522,569-80,527,880 SEMA3C
    nsv6829994copy number variation1nstd229human GRCh38 chr7: 80,572,401-80,747,100 , GRCh37.p13 chr7: 80,201,717-80,376,416 CD36, SEMA3C
    nsv6828715copy number variation1nstd229human GRCh38 chr7: 80,675,208-80,793,905 , GRCh37.p13 chr7: 80,304,524-80,423,221 CD36, SEMA3C
    nsv6827348copy number variation1nstd229human GRCh38 chr7: 80,851,183-80,878,474 , GRCh37.p13 chr7: 80,480,499-80,507,790 SEMA3C
    nsv6826518copy number variation1nstd229human GRCh38 chr7: 80,871,301-80,879,200 , GRCh37.p13 chr7: 80,500,617-80,508,516 SEMA3C
    nsv6826202copy number variation1nstd229human GRCh38 chr7: 80,829,256-80,887,529 , GRCh37.p13 chr7: 80,458,572-80,516,845 SEMA3C
    nsv6826149copy number variation1nstd229human GRCh38 chr7: 80,672,975-81,115,150 , GRCh37.p13 chr7: 80,302,291-80,744,466 CD36, SEMA3C
    nsv6822998copy number variation1nstd229human GRCh38 chr7: 80,843,101-80,852,100 , GRCh37.p13 chr7: 80,472,417-80,481,416 SEMA3C
    nsv6822979copy number variation1nstd229human GRCh38 chr7: 80,876,096-80,880,743 , GRCh37.p13 chr7: 80,505,412-80,510,059 SEMA3C
    nsv6822429copy number variation1nstd229human GRCh38 chr7: 80,671,603-80,763,130 , GRCh37.p13 chr7: 80,300,919-80,392,446 CD36, SEMA3C
    nsv6821752copy number variation1nstd229human GRCh38 chr7: 80,695,906-80,835,562 , GRCh37.p13 chr7: 80,325,222-80,464,878 SEMA3C
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