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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
    nsv7098887copy number variation1nstd102humanPathogenic GRCh37 chr10: 93,249,133-97,616,970 , GRCh38.p12 chr10: 91,489,376-95,857,213 LGI1, LOC107984257, 79 more genes
    nsv7073775inversion1nstd229human GRCh38 chr10: 92,205,149-92,554,453 , GRCh37.p13 chr10: 93,964,906-94,314,210 MARK2P9, RNY3P12, 4 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6897307copy number variation1nstd229human GRCh38 chr10: 91,929,909-92,166,613 , GRCh37.p13 chr10: 93,689,666-93,926,370 BTAF1, SDHCP2, 3 more genes
    nsv6896867copy number variation1nstd229human GRCh38 chr10: 92,194,822-92,200,268 , GRCh37.p13 chr10: 93,954,579-93,960,025 CPEB3
    nsv6895658copy number variation1nstd229human GRCh38 chr10: 92,263,301-92,275,012 , GRCh37.p13 chr10: 94,023,058-94,034,769 CPEB3
    nsv6894969copy number variation1nstd229human GRCh38 chr10: 92,147,333-92,150,050 , GRCh37.p13 chr10: 93,907,090-93,909,807 CPEB3
    nsv6894393copy number variation1nstd229human GRCh38 chr10: 92,101,562-92,101,949 , GRCh37.p13 chr10: 93,861,319-93,861,706 CPEB3
    nsv6892927copy number variation1nstd229human GRCh38 chr10: 92,248,438-92,253,837 , GRCh37.p13 chr10: 94,008,195-94,013,594 CPEB3
    nsv6892751copy number variation1nstd229human GRCh38 chr10: 92,278,772-92,288,042 , GRCh37.p13 chr10: 94,038,529-94,047,799 CPEB3
    nsv6892701copy number variation1nstd229human GRCh38 chr10: 92,199,624-92,205,183 , GRCh37.p13 chr10: 93,959,381-93,964,940 CPEB3
    nsv6892016copy number variation1nstd229human GRCh38 chr10: 92,235,895-92,238,767 , GRCh37.p13 chr10: 93,995,652-93,998,524 CPEB3
    nsv6891248copy number variation1nstd229human GRCh38 chr10: 92,128,601-92,142,100 , GRCh37.p13 chr10: 93,888,358-93,901,857 EIF4A1P8, CPEB3
    nsv6890991copy number variation1nstd229human GRCh38 chr10: 92,259,382-92,263,420 , GRCh37.p13 chr10: 94,019,139-94,023,177 CPEB3
    nsv6888920copy number variation1nstd229human GRCh38 chr10: 92,197,901-92,222,700 , GRCh37.p13 chr10: 93,957,658-93,982,457 NHP2P1, CPEB3
    nsv6888027copy number variation1nstd229human GRCh38 chr10: 92,170,817-92,171,220 , GRCh37.p13 chr10: 93,930,574-93,930,977 CPEB3
    nsv6886977copy number variation1nstd229human GRCh38 chr10: 92,265,106-92,280,247 , GRCh37.p13 chr10: 94,024,863-94,040,004 CPEB3
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