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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143939copy number variation1nstd232human GRCh37.p13 chr10: 33,097,530-33,097,588 , GRCh38.p12 chr10: 32,808,602-32,808,660 CCDC7
    nsv7140273insertion1nstd232human GRCh37.p13 chr10: 32,936,398-32,936,398 , GRCh38.p12 chr10: 32,647,470-32,647,470 CCDC7
    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
    nsv7076871inversion1nstd229human GRCh38 chr10: 32,526,761-32,535,321 , GRCh37.p13 chr10: 32,815,689-32,824,249 CCDC7
    nsv7076376inversion1nstd229human GRCh38 chr10: 32,796,964-32,801,411 , GRCh37.p13 chr10: 33,085,892-33,090,339 CCDC7
    nsv7074720inversion1nstd229human GRCh38 chr10: 32,479,470-32,574,701 , GRCh37.p13 chr10: 32,768,398-32,863,629 CCDC7, C1DP1
    nsv7072978inversion1nstd229human GRCh38 chr10: 32,766,151-32,767,667 , GRCh37.p13 chr10: 33,055,079-33,056,595 CCDC7
    nsv7071918inversion1nstd229human GRCh38 chr10: 32,763,676-32,766,289 , GRCh37.p13 chr10: 33,052,604-33,055,217 CCDC7
    nsv7070551inversion1nstd229human GRCh38 chr10: 32,654,431-32,654,520 , GRCh37.p13 chr10: 32,943,359-32,943,448 CCDC7
    nsv7070496inversion1nstd229human GRCh38 chr10: 32,528,359-32,615,453 , GRCh37.p13 chr10: 32,817,287-32,904,381 CCDC7
    nsv7068993inversion1nstd229human GRCh38 chr10: 32,600,951-32,601,014 , GRCh37.p13 chr10: 32,889,879-32,889,942 CCDC7
    nsv7065771inversion1nstd229human GRCh38 chr10: 32,766,155-32,767,666 , GRCh37.p13 chr10: 33,055,083-33,056,594 CCDC7
    nsv7065010inversion1nstd229human GRCh38 chr10: 32,699,822-35,479,064 , GRCh37.p13 chr10: 32,988,750-35,767,992 RNU6-1167P, MIR3611, 34 more genes
    nsv7061942inversion1nstd229human GRCh38 chr10: 32,596,736-32,755,057 , GRCh37.p13 chr10: 32,885,664-33,043,985 CCDC7
    nsv6897632copy number variation1nstd229human GRCh38 chr10: 32,520,880-32,611,560 , GRCh37.p13 chr10: 32,809,808-32,900,488 CCDC7
    nsv6897472copy number variation1nstd229human GRCh38 chr10: 32,639,888-32,655,273 , GRCh37.p13 chr10: 32,928,816-32,944,201 CCDC7
    nsv6897302copy number variation1nstd229human GRCh38 chr10: 32,494,028-32,497,657 , GRCh37.p13 chr10: 32,782,956-32,786,585 CCDC7
    nsv6896528copy number variation1nstd229human GRCh38 chr10: 32,713,500-32,715,733 , GRCh37.p13 chr10: 33,002,428-33,004,661 CCDC7
    nsv6896361copy number variation1nstd229human GRCh38 chr10: 32,709,940-32,721,160 , GRCh37.p13 chr10: 32,998,868-33,010,088 CCDC7
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