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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140334copy number variation1nstd232human GRCh37.p13 chr10: 114,877,143-114,877,192 , GRCh38.p12 chr10: 113,117,384-113,117,433 TCF7L2
    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
    nsv7065227inversion1nstd229human GRCh38 chr10: 113,127,602-113,127,656 , GRCh37.p13 chr10: 114,887,361-114,887,415 TCF7L2
    nsv7063112inversion1nstd229human GRCh38 chr10: 113,102,756-113,110,847 , GRCh37.p13 chr10: 114,862,515-114,870,606 TCF7L2
    nsv6896716copy number variation1nstd229human GRCh38 chr10: 113,013,819-113,014,302 , GRCh37.p13 chr10: 114,773,578-114,774,061 TCF7L2
    nsv6896165copy number variation1nstd229human GRCh38 chr10: 112,978,555-113,018,200 , GRCh37.p13 chr10: 114,738,314-114,777,959 RPS15AP30, TCF7L2
    nsv6895600copy number variation1nstd229human GRCh38 chr10: 113,149,671-113,149,760 , GRCh37.p13 chr10: 114,909,430-114,909,519 TCF7L2
    nsv6894253copy number variation1nstd229human GRCh38 chr10: 113,008,029-113,008,187 , GRCh37.p13 chr10: 114,767,788-114,767,946 TCF7L2
    nsv6894159copy number variation1nstd229human GRCh38 chr10: 112,985,101-112,989,700 , GRCh37.p13 chr10: 114,744,860-114,749,459 RPS15AP30, TCF7L2
    nsv6894000copy number variation1nstd229human GRCh38 chr10: 112,953,110-112,968,261 , GRCh37.p13 chr10: 114,712,869-114,728,020 TCF7L2
    nsv6893906copy number variation1nstd229human GRCh38 chr10: 112,951,401-112,951,600 , GRCh37.p13 chr10: 114,711,160-114,711,359 TCF7L2
    nsv6893875copy number variation1nstd229human GRCh38 chr10: 112,972,461-112,976,179 , GRCh37.p13 chr10: 114,732,220-114,735,938 TCF7L2
    nsv6893667copy number variation1nstd229human GRCh38 chr10: 113,019,401-113,023,400 , GRCh37.p13 chr10: 114,779,160-114,783,159 TCF7L2
    nsv6891266copy number variation1nstd229human GRCh38 chr10: 113,006,621-113,009,758 , GRCh37.p13 chr10: 114,766,380-114,769,517 TCF7L2
    nsv6890494copy number variation1nstd229human GRCh38 chr10: 113,072,615-113,075,726 , GRCh37.p13 chr10: 114,832,374-114,835,485 TCF7L2
    nsv6890087copy number variation1nstd229human GRCh38 chr10: 113,057,101-113,074,371 , GRCh37.p13 chr10: 114,816,860-114,834,130 TCF7L2
    nsv6889622copy number variation1nstd229human GRCh38 chr10: 112,972,077-112,973,864 , GRCh37.p13 chr10: 114,731,836-114,733,623 TCF7L2
    nsv6888687copy number variation1nstd229human GRCh38 chr10: 112,989,220-112,992,992 , GRCh37.p13 chr10: 114,748,979-114,752,751 TCF7L2
    nsv6886922copy number variation1nstd229human GRCh38 chr10: 113,079,804-113,085,048 , GRCh37.p13 chr10: 114,839,563-114,844,807 TCF7L2
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