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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
    nsv7093656copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,697,798-90,767,614 , GRCh38.p12 chr10: 88,938,041-89,007,857 ACTA2, FAS-AS1, 2 more genes
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073898inversion1nstd229human GRCh38 chr10: 85,457,267-89,078,986 , GRCh37.p13 chr10: 87,217,024-90,838,743 LOC112268064, LOC105378416, 74 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
    nsv6893552copy number variation1nstd229human GRCh38 chr10: 88,916,193-88,941,657 , GRCh37.p13 chr10: 90,675,950-90,701,414 ACTA2-AS1, STAMBPL1, 1 more genes
    nsv6893510copy number variation1nstd229human GRCh38 chr10: 88,357,217-89,008,456 , GRCh37.p13 chr10: 90,116,974-90,768,213 PTCD2P2, ACTA2, 16 more genes
    nsv6891834copy number variation1nstd229human GRCh38 chr10: 88,935,360-88,938,060 , GRCh37.p13 chr10: 90,695,117-90,697,817 ACTA2-AS1, ACTA2
    nsv6890427copy number variation1nstd229human GRCh38 chr10: 88,917,949-88,975,071 , GRCh37.p13 chr10: 90,677,706-90,734,828 STAMBPL1, ACTA2, 2 more genes
    nsv6884066copy number variation1nstd229human GRCh38 chr10: 88,937,099-88,937,187 , GRCh37.p13 chr10: 90,696,856-90,696,944 ACTA2-AS1, ACTA2
    nsv6883259copy number variation1nstd229human GRCh38 chr10: 88,909,886-89,428,064 , GRCh37.p13 chr10: 90,669,643-91,187,821 IFIT2, STAMBPL1, 18 more genes
    nsv6883136copy number variation1nstd229human GRCh38 chr10: 88,943,909-88,947,257 , GRCh37.p13 chr10: 90,703,666-90,707,014 ACTA2
    nsv6881829copy number variation1nstd229human GRCh38 chr10: 88,960,681-88,960,721 , GRCh37.p13 chr10: 90,720,438-90,720,478 ACTA2
    nsv6881199copy number variation1nstd229human GRCh38 chr10: 88,487,671-89,149,734 , GRCh37.p13 chr10: 90,247,428-90,909,491 PTCD2P2, LOC100289238, 18 more genes
    nsv6880304copy number variation1nstd229human GRCh38 chr10: 88,955,085-88,962,971 , GRCh37.p13 chr10: 90,714,842-90,722,728 ACTA2
    nsv6878824copy number variation1nstd229human GRCh38 chr10: 88,958,205-88,963,847 , GRCh37.p13 chr10: 90,717,962-90,723,604 ACTA2
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637707copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,672,265-91,165,763 , GRCh38.p12 chr10: 88,912,508-89,406,006 IFIT1, IFIT3, 16 more genes
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