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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
    nsv7075171inversion1nstd229human GRCh38 chr10: 16,344,428-16,531,956 , GRCh37.p13 chr10: 16,386,427-16,573,955 C1QL3, RNU2-18P, 1 more genes
    nsv7074683inversion1nstd229human GRCh38 chr10: 16,451,959-16,459,146 , GRCh37.p13 chr10: 16,493,958-16,501,145 PTER
    nsv7072491inversion1nstd229human GRCh38 chr10: 16,461,276-16,461,295 , GRCh37.p13 chr10: 16,503,275-16,503,294 PTER
    nsv7069701inversion1nstd229human GRCh38 chr10: 16,478,068-16,478,087 , GRCh37.p13 chr10: 16,520,067-16,520,086 PTER
    nsv7067038inversion1nstd229human GRCh38 chr10: 16,439,285-16,445,430 , GRCh37.p13 chr10: 16,481,284-16,487,429 PTER
    nsv6896863copy number variation1nstd229human GRCh38 chr10: 16,384,901-16,532,000 , GRCh37.p13 chr10: 16,426,900-16,573,999 PTER, RNU2-18P, 1 more genes
    nsv6895834copy number variation1nstd229human GRCh38 chr10: 16,498,176-16,498,543 , GRCh37.p13 chr10: 16,540,175-16,540,542 PTER
    nsv6895776copy number variation1nstd229human GRCh38 chr10: 16,449,440-16,457,247 , GRCh37.p13 chr10: 16,491,439-16,499,246 PTER
    nsv6895380copy number variation1nstd229human GRCh38 chr10: 16,445,931-16,449,469 , GRCh37.p13 chr10: 16,487,930-16,491,468 PTER
    nsv6891579copy number variation1nstd229human GRCh38 chr10: 16,473,477-16,476,466 , GRCh37.p13 chr10: 16,515,476-16,518,465 PTER, RNU2-18P
    nsv6889844copy number variation1nstd229human GRCh38 chr10: 16,468,115-16,474,126 , GRCh37.p13 chr10: 16,510,114-16,516,125 PTER, RNU2-18P
    nsv6889201copy number variation1nstd229human GRCh38 chr10: 16,456,787-16,457,181 , GRCh37.p13 chr10: 16,498,786-16,499,180 PTER
    nsv6886223copy number variation1nstd229human GRCh38 chr10: 16,497,213-16,501,210 , GRCh37.p13 chr10: 16,539,212-16,543,209 PTER
    nsv6885848copy number variation1nstd229human GRCh38 chr10: 16,496,217-16,496,269 , GRCh37.p13 chr10: 16,538,216-16,538,268 PTER
    nsv6885183copy number variation1nstd229human GRCh38 chr10: 16,515,950-16,519,876 , GRCh37.p13 chr10: 16,557,949-16,561,875 C1QL3, PTER
    nsv6884317copy number variation1nstd229human GRCh38 chr10: 16,451,801-16,455,200 , GRCh37.p13 chr10: 16,493,800-16,497,199 PTER
    nsv6882050copy number variation1nstd229human GRCh38 chr10: 16,509,064-16,511,220 , GRCh37.p13 chr10: 16,551,063-16,553,219 PTER
    nsv6880850copy number variation1nstd229human GRCh38 chr10: 16,493,556-16,502,874 , GRCh37.p13 chr10: 16,535,555-16,544,873 PTER
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