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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148238copy number variation1nstd102humanPathogenic GRCh38 chr8: 115,586,904-135,607,135 , GRCh37.p13 chr8: 116,599,131-136,619,378 CCDC26, EFR3A, 238 more genes
    nsv7148124copy number variation1nstd102humanPathogenic GRCh37 chr8: 118,185,471-126,635,744 , GRCh38.p12 chr8: 117,173,232-125,623,500 LINC02964, TATDN1, 115 more genes
    nsv7097417copy number variation1nstd102humanUncertain significance GRCh37 chr8: 118,811,951-120,844,804 , GRCh38.p12 chr8: 117,799,712-119,832,564 TAF2, SAMD12-AS1, 23 more genes
    nsv7097416copy number variation1nstd102humanPathogenic GRCh37 chr8: 117,859,739-120,844,804 , GRCh38.p12 chr8: 116,847,500-119,832,564 SAMD12, LOC105375717, 38 more genes
    nsv7097415copy number variation1nstd102humanUncertain significance GRCh37 chr8: 117,647,788-120,797,526 , GRCh38.p12 chr8: 116,635,549-119,785,286 LOC100286746, LOC105375717, 40 more genes
    nsv7074355inversion1nstd229human GRCh38 chr8: 119,640,142-119,644,457 , GRCh37.p13 chr8: 120,652,382-120,656,697 ENPP2
    nsv7072142inversion1nstd229human GRCh38 chr8: 113,332,988-120,659,210 , GRCh37.p13 chr8: 114,345,217-121,671,450 ENPP2, RAD21-AS1, 67 more genes
    nsv7066383inversion1nstd229human GRCh38 chr8: 119,659,491-119,659,508 , GRCh37.p13 chr8: 120,671,731-120,671,748 ENPP2
    nsv7060798inversion1nstd229human GRCh38 chr8: 119,582,102-119,582,349 , GRCh37.p13 chr8: 120,594,342-120,594,589 ENPP2
    nsv7060535inversion1nstd229human GRCh38 chr8: 119,610,492-119,615,918 , GRCh37.p13 chr8: 120,622,732-120,628,158 ENPP2
    nsv7060402inversion1nstd229human GRCh38 chr8: 119,632,604-119,634,220 , GRCh37.p13 chr8: 120,644,844-120,646,460 ENPP2
    nsv7060085inversion1nstd229human GRCh38 chr8: 119,567,940-119,567,977 , GRCh37.p13 chr8: 120,580,180-120,580,217 ENPP2
    nsv7059708inversion1nstd229human GRCh38 chr8: 119,264,677-119,776,203 , GRCh37.p13 chr8: 120,276,917-120,788,443 CCN3, ENPP2, 6 more genes
    nsv6857809copy number variation1nstd229human GRCh38 chr8: 119,638,601-119,641,800 , GRCh37.p13 chr8: 120,650,841-120,654,040 ENPP2
    nsv6848660copy number variation1nstd229human GRCh38 chr8: 119,341,601-119,557,400 , GRCh37.p13 chr8: 120,353,841-120,569,640 LOC392264, ENPP2, 1 more genes
    nsv6846076copy number variation1nstd229human GRCh38 chr8: 119,628,670-119,632,984 , GRCh37.p13 chr8: 120,640,910-120,645,224 ENPP2
    nsv6844888copy number variation1nstd229human GRCh38 chr8: 119,660,926-119,670,544 , GRCh37.p13 chr8: 120,673,166-120,682,784 ENPP2, LOC105375727
    nsv6843486copy number variation1nstd229human GRCh38 chr8: 119,633,442-119,633,960 , GRCh37.p13 chr8: 120,645,682-120,646,200 ENPP2
    nsv6841751copy number variation1nstd229human GRCh38 chr8: 119,300,634-119,949,091 , GRCh37.p13 chr8: 120,312,874-120,961,331 LOC105375727, CYCSP23, 11 more genes
    nsv6839091copy number variation1nstd229human GRCh38 chr8: 119,620,669-119,621,054 , GRCh37.p13 chr8: 120,632,909-120,633,294 ENPP2
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