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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
    nsv7093904copy number variation1nstd102humanUncertain significance GRCh37 chr10: 99,344,461-105,992,004 , GRCh38.p12 chr10: 97,584,704-104,232,246 ABCC2, LBX1-AS1, 160 more genes
    nsv7093855copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,987,027-103,384,587 , GRCh38.p12 chr10: 101,227,270-101,624,830 RNU2-43P, BTRC, 11 more genes
    nsv7093699copy number variation1nstd102humanUncertain significance GRCh37 chr10: 102,747,968-103,535,657 , GRCh38.p12 chr10: 100,988,211-101,775,900 RNY5P7, TLX1, 25 more genes
    nsv7070234inversion1nstd229human GRCh38 chr10: 101,670,169-101,670,185 , GRCh37.p13 chr10: 103,429,926-103,429,942 FBXW4
    nsv7061391inversion1nstd229human GRCh38 chr10: 100,357,388-105,969,995 , GRCh37.p13 chr10: 102,117,145-107,729,753 , CALHM1, 127 more genes
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6897727copy number variation1nstd229human GRCh38 chr10: 101,666,701-101,878,800 , GRCh37.p13 chr10: 103,426,458-103,638,557 , LOC105378457, 10 more genes
    nsv6897208copy number variation1nstd229human GRCh38 chr10: 101,621,417-101,623,520 , GRCh37.p13 chr10: 103,381,174-103,383,277 RNU6-1165P, FBXW4
    nsv6897057copy number variation1nstd229human GRCh38 chr10: 101,653,801-101,656,500 , GRCh37.p13 chr10: 103,413,558-103,416,257 FBXW4
    nsv6894677copy number variation1nstd229human GRCh38 chr10: 101,635,729-101,641,638 , GRCh37.p13 chr10: 103,395,486-103,401,395 FBXW4
    nsv6894560copy number variation1nstd229human GRCh38 chr10: 101,661,984-101,689,104 , GRCh37.p13 chr10: 103,421,741-103,448,861 FBXW4
    nsv6891843copy number variation1nstd229human GRCh38 chr10: 101,586,386-101,633,544 , GRCh37.p13 chr10: 103,346,143-103,393,301 FBXW4, MIR3158-1, 4 more genes
    nsv6889052copy number variation1nstd229human GRCh38 chr10: 101,373,162-101,631,853 , GRCh37.p13 chr10: 103,132,919-103,391,610 POLL, RNU6-1165P, 5 more genes
    nsv6887935copy number variation1nstd229human GRCh38 chr10: 101,628,062-101,631,112 , GRCh37.p13 chr10: 103,387,819-103,390,869 FBXW4
    nsv6886789copy number variation1nstd229human GRCh38 chr10: 101,627,789-101,628,102 , GRCh37.p13 chr10: 103,387,546-103,387,859 FBXW4
    nsv6886375copy number variation1nstd229human GRCh38 chr10: 101,685,868-101,686,534 , GRCh37.p13 chr10: 103,445,625-103,446,291 FBXW4
    nsv6886100copy number variation1nstd229human GRCh38 chr10: 101,648,497-101,648,822 , GRCh37.p13 chr10: 103,408,254-103,408,579 FBXW4
    nsv6884582copy number variation1nstd229human GRCh38 chr10: 101,634,718-101,635,279 , GRCh37.p13 chr10: 103,394,475-103,395,036 FBXW4
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