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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7060207inversion1nstd229human GRCh38 chr8: 143,324,640-143,375,537 , GRCh37.p13 chr8: 144,406,810-144,457,707 RNU6-220P, RHPN1, 2 more genes
    nsv6872281copy number variation1nstd229human GRCh38 chr8: 143,383,201-143,408,300 , GRCh37.p13 chr8: 144,465,371-144,490,470 RHPN1
    nsv6872033copy number variation1nstd229human GRCh38 chr8: 143,381,375-143,423,488 , GRCh37.p13 chr8: 144,463,545-144,505,658 RHPN1, MAFA-AS1, 1 more genes
    nsv6871840copy number variation1nstd229human GRCh38 chr8: 143,273,127-143,593,659 , GRCh37.p13 chr8: 144,355,297-144,675,829 MAFA-AS1, SNORD149, 16 more genes
    nsv6870026copy number variation1nstd229human GRCh38 chr8: 143,358,701-143,389,700 , GRCh37.p13 chr8: 144,440,871-144,471,870 TOP1MT, RHPN1-AS1, 1 more genes
    nsv6860477copy number variation1nstd229human GRCh38 chr8: 143,358,718-143,389,695 , GRCh37.p13 chr8: 144,440,888-144,471,865 TOP1MT, RHPN1-AS1, 1 more genes
    nsv6860178copy number variation1nstd229human GRCh38 chr8: 143,332,697-143,396,956 , GRCh37.p13 chr8: 144,414,867-144,479,126 RHPN1-AS1, RNU6-220P, 2 more genes
    nsv6637661copy number variation1nstd102humanUncertain significance GRCh37 chr8: 143,895,666-144,568,446 , GRCh38.p12 chr8: 142,814,250-143,486,276 LY6L, ZC3H3, 26 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632758copy number variation3nstd224human GRCh37 chr8: 144,446,285-144,464,795 , GRCh38.p12 chr8: 143,364,115-143,382,625 RHPN1-AS1, RHPN1
    nsv6632681copy number variation1nstd224human GRCh37 chr8: 144,403,532-144,624,438 , GRCh38.p12 chr8: 143,321,362-143,542,268 RHPN1, MAFA, 8 more genes
    nsv6632503copy number variation1nstd224human GRCh37 chr8: 144,303,418-144,547,942 , GRCh38.p12 chr8: 143,221,248-143,465,772 GLI4, RHPN1-AS1, 10 more genes
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
    nsv6425791copy number variation1nstd223human GRCh38 chr8: 142,975,701-144,021,300 , GRCh37.p13 chr8: 144,057,118-144,743,525 LY6H, RHPN1-AS1, 55 more genes
    nsv6424965copy number variation1nstd223human GRCh38 chr8: 143,382,646-143,441,000 , GRCh37.p13 chr8: 144,464,816-144,523,170 RHPN1, ZC3H3, 3 more genes
    nsv6424504copy number variation1nstd223human GRCh38 chr8: 143,313,874-143,370,654 , GRCh37.p13 chr8: 144,396,044-144,452,824 TOP1MT, RHPN1-AS1, 2 more genes
    nsv6419786copy number variation1nstd223human GRCh38 chr8: 143,358,718-143,389,691 , GRCh37.p13 chr8: 144,440,888-144,471,861 TOP1MT, RHPN1, 1 more genes
    nsv6315406copy number variation1nstd102humanPathogenic GRCh37 chr8: 84,712,253-146,295,771 , GRCh38.p12 chr8: 83,800,018-145,070,385 RHPN1, RPL18P7, 833 more genes
    nsv6314744copy number variation1nstd102humanPathogenic GRCh37 chr8: 96,496,503-146,295,711 , GRCh38.p12 chr8: 95,484,275-145,070,325 OSR2, LOC392268, 676 more genes
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