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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5911366copy number variation1nstd209human GRCh38 chr10: 42,494,832-42,494,977 , GRCh37.p13 chr10: 42,990,280-42,990,425 LINC00839
    nsv5856379copy number variation1nstd209human GRCh38 chr10: 42,445,076-42,480,161 , GRCh37.p13 chr10: 42,940,524-42,975,609 CCNYL2, LINC00839
    nsv5490890copy number variation1nstd206human GRCh38 chr10: 42,480,918-42,481,230 , GRCh37.p13 chr10: 42,976,366-42,976,678 LINC00839
    nsv5489087copy number variation1nstd206human GRCh38 chr10: 42,177,458-42,632,385 , GRCh37.p13 chr10: 42,672,906-43,127,833 LINC00839, FXYD6P1, 10 more genes
    nsv5488943copy number variation1nstd206human GRCh38 chr10: 42,067,000-42,558,265 , GRCh37.p13 chr10: 42,598,688-43,053,713 ZNF37BP, LOC105378267, 8 more genes
    nsv5485460copy number variation1nstd206human GRCh38 chr10: 42,481,360-42,481,939 , GRCh37.p13 chr10: 42,976,808-42,977,387 LINC00839
    nsv5481453copy number variation1nstd206human GRCh38 chr10: 42,337,265-42,538,265 , GRCh37.p13 chr10: 42,832,713-43,033,713 ZNF37BP, CCNYL2, 2 more genes
    nsv5479422copy number variation1nstd206human GRCh38 chr10: 42,470,059-42,478,480 , GRCh37.p13 chr10: 42,965,507-42,973,928 CCNYL2, LINC00839
    nsv5364890translocation1nstd200human GRCh38 chr10: 42,487,132-42,487,132 , GRCh38 chr10: 42,644,385-42,644,385 , GRCh37.p13 chr10: 42,982,580-42,982,580 , GRCh37.p13 chr10: 43,139,833-43,139,833 LINC00839, LOC105378268
    nsv5134261mobile element insertion1nstd203human GRCh38 chr10: 42,484,118-42,484,137 , GRCh37.p13 chr10: 42,979,566-42,979,585 LINC00839
    nsv5035636inversion1nstd200human GRCh38 chr10: 32,580,256-50,959,654 , GRCh37.p13 chr10: 32,869,184-52,719,414 , ZNF32-AS2, 320 more genes
    nsv5033632inversion1nstd200human GRCh38 chr10: 36,819,152-58,318,428 , GRCh37.p13 chr10: 37,108,080-60,078,188 , LOC107001062, 306 more genes
    nsv4989033copy number variation1nstd200human GRCh38 chr10: 42,177,453-42,632,445 , GRCh37.p13 chr10: 42,672,901-43,127,893 ZNF33B, ZNF37BP, 10 more genes
    nsv4989029copy number variation1nstd200human GRCh38 chr10: 42,103,130-42,919,644 , GRCh37.p13 chr10: 42,598,578-43,415,092 LOC105378267, BMS1, 23 more genes
    nsv4969727copy number variation1nstd200human GRCh38 chr10: 42,493,922-42,493,982 , GRCh37.p13 chr10: 42,989,370-42,989,430 LINC00839
    nsv4870857inversion1nstd200human GRCh37 chr10: 37,108,081-60,078,188 , GRCh38.p12 chr10: 36,819,153-58,318,428 , NCOA4, 306 more genes
    nsv4841602copy number variation1nstd200human GRCh37 chr10: 42,968,333-42,969,477 , GRCh38.p12 chr10: 42,472,885-42,474,029 LINC00839
    nsv4837971copy number variation1nstd200human GRCh37 chr10: 42,990,280-42,990,428 , GRCh38.p12 chr10: 42,494,832-42,494,980 LINC00839
    nsv4617801copy number variation1nstd183human GRCh37 chr10: 42,820,178-43,090,218 , GRCh38.p12 chr10: 42,324,730-42,594,770 ZNF33B, LINC00839, 5 more genes
    nsv4527125copy number variation1nstd166human GRCh37.p13 chr10: 42,980,651-42,981,191 , GRCh38.p12 chr10: 42,485,203-42,485,743 LINC00839
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