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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141903insertion1nstd232human GRCh37.p13 chr10: 101,574,413-101,574,413 , GRCh38.p12 chr10: 99,814,656-99,814,656 ABCC2
    nsv7137465copy number variation1nstd232human GRCh37.p13 chr10: 101,574,280-101,574,337 , GRCh38.p12 chr10: 99,814,523-99,814,580 ABCC2
    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
    nsv7073103inversion1nstd229human GRCh38 chr10: 99,802,163-99,802,237 , GRCh37.p13 chr10: 101,561,920-101,561,994 ABCC2
    nsv7059886inversion1nstd229human GRCh38 chr10: 95,520,399-102,687,169 , GRCh37.p13 chr10: 97,280,156-104,446,926 , ENTPD1-AS1, 168 more genes
    nsv6898026copy number variation1nstd229human GRCh38 chr10: 99,791,875-99,801,964 , GRCh37.p13 chr10: 101,551,632-101,561,721 ABCC2
    nsv6897773copy number variation1nstd229human GRCh38 chr10: 99,802,101-99,805,600 , GRCh37.p13 chr10: 101,561,858-101,565,357 ABCC2
    nsv6895916copy number variation1nstd229human GRCh38 chr10: 99,831,125-99,888,845 , GRCh37.p13 chr10: 101,590,882-101,648,602 DNMBP, ABCC2
    nsv6893077copy number variation1nstd229human GRCh38 chr10: 99,808,782-99,845,296 , GRCh37.p13 chr10: 101,568,539-101,605,053 ABCC2
    nsv6893009copy number variation1nstd229human GRCh38 chr10: 99,801,858-99,802,084 , GRCh37.p13 chr10: 101,561,615-101,561,841 ABCC2
    nsv6891126copy number variation1nstd229human GRCh38 chr10: 99,834,952-99,835,103 , GRCh37.p13 chr10: 101,594,709-101,594,860 ABCC2
    nsv6891000copy number variation1nstd229human GRCh38 chr10: 99,803,892-99,808,735 , GRCh37.p13 chr10: 101,563,649-101,568,492 ABCC2
    nsv6889370copy number variation1nstd229human GRCh38 chr10: 99,776,801-99,780,800 , GRCh37.p13 chr10: 101,536,558-101,540,557 ABCC2
    nsv6888299copy number variation1nstd229human GRCh38 chr10: 99,803,801-99,813,300 , GRCh37.p13 chr10: 101,563,558-101,573,057 ABCC2
    nsv6886739copy number variation1nstd229human GRCh38 chr10: 99,811,124-99,814,984 , GRCh37.p13 chr10: 101,570,881-101,574,741 ABCC2
    nsv6880127copy number variation1nstd229human GRCh38 chr10: 99,711,540-100,023,720 , GRCh37.p13 chr10: 101,471,297-101,783,477 NANOGP6, ENTPD7, 5 more genes
    nsv6879951copy number variation1nstd229human GRCh38 chr10: 99,778,221-99,786,938 , GRCh37.p13 chr10: 101,537,978-101,546,695 NANOGP6, ABCC2
    nsv6878537copy number variation1nstd229human GRCh38 chr10: 99,832,151-99,832,208 , GRCh37.p13 chr10: 101,591,908-101,591,965 ABCC2
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