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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
    nsv7093801copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,671,314-79,799,964 , GRCh38.p12 chr10: 73,911,556-78,040,206 COMTD1, DUSP13B, 53 more genes
    nsv7093731copy number variation1nstd102humanPathogenic GRCh37 chr10: 76,349,020-78,317,046 , GRCh38.p12 chr10: 74,589,262-76,557,288 ADK, SAMD8, 25 more genes
    nsv7093650copy number variation1nstd102humanLikely benign GRCh37 chr10: 76,736,352-77,198,536 , GRCh38.p12 chr10: 74,976,594-75,438,778 VDAC2, COMTD1, 16 more genes
    nsv7070698inversion1nstd229human GRCh38 chr10: 75,772,696-75,772,729 , GRCh37.p13 chr10: 77,532,454-77,532,487 LRMDA
    nsv7070564inversion1nstd229human GRCh38 chr10: 75,482,129-75,493,931 , GRCh37.p13 chr10: 77,241,887-77,253,689 LRMDA
    nsv7070467inversion1nstd229human GRCh38 chr10: 76,540,426-76,546,751 , GRCh37.p13 chr10: 78,300,184-78,306,509 LRMDA
    nsv7069255inversion1nstd229human GRCh38 chr10: 75,886,103-75,891,622 , GRCh37.p13 chr10: 77,645,861-77,651,380 LRMDA
    nsv7067692inversion1nstd229human GRCh38 chr10: 76,260,948-76,263,306 , GRCh37.p13 chr10: 78,020,706-78,023,064 RNU6-673P, LRMDA
    nsv7067392inversion1nstd229human GRCh38 chr10: 75,751,944-75,756,296 , GRCh37.p13 chr10: 77,511,702-77,516,054 LRMDA
    nsv7065281inversion1nstd229human GRCh38 chr10: 76,099,577-76,100,940 , GRCh37.p13 chr10: 77,859,335-77,860,698 LRMDA
    nsv7063069inversion1nstd229human GRCh38 chr10: 75,019,895-76,543,360 , GRCh37.p13 chr10: 76,779,653-78,303,118 SAMD8, LOC105378367, 21 more genes
    nsv7062174inversion1nstd229human GRCh38 chr10: 76,145,360-76,476,424 , GRCh37.p13 chr10: 77,905,118-78,236,182 RNU6-673P, RN7SL518P, 2 more genes
    nsv7061590inversion1nstd229human GRCh38 chr10: 76,040,356-76,043,500 , GRCh37.p13 chr10: 77,800,114-77,803,258 LRMDA
    nsv7060637inversion1nstd229human GRCh38 chr10: 76,033,142-76,038,397 , GRCh37.p13 chr10: 77,792,900-77,798,155 LRMDA
    nsv7059903inversion1nstd229human GRCh38 chr10: 75,481,949-75,488,336 , GRCh37.p13 chr10: 77,241,707-77,248,094 LRMDA
    nsv6897972copy number variation1nstd229human GRCh38 chr10: 75,826,771-75,826,943 , GRCh37.p13 chr10: 77,586,529-77,586,701 LRMDA
    nsv6897860copy number variation1nstd229human GRCh38 chr10: 75,833,416-75,833,452 , GRCh37.p13 chr10: 77,593,174-77,593,210 LRMDA
    nsv6897780copy number variation1nstd229human GRCh38 chr10: 75,779,588-75,782,206 , GRCh37.p13 chr10: 77,539,346-77,541,964 LRMDA
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