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Items: 1 to 20 of 242

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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
    nsv7069665inversion1nstd229human GRCh38 chr8: 143,272,120-143,281,371 , GRCh37.p13 chr8: 144,354,290-144,363,541 GLI4, MINCR
    nsv6874810copy number variation1nstd229human GRCh38 chr8: 143,265,672-143,265,810 , GRCh37.p13 chr8: 144,347,842-144,347,980 GLI4
    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
    nsv6867072copy number variation1nstd229human GRCh38 chr8: 143,242,548-143,329,567 , GRCh37.p13 chr8: 144,324,718-144,411,737 GLI4, MINCR, 3 more genes
    nsv6863820copy number variation1nstd229human GRCh38 chr8: 143,257,130-143,275,021 , GRCh37.p13 chr8: 144,339,300-144,357,191 GLI4, ZFP41
    nsv6860374copy number variation1nstd229human GRCh38 chr8: 143,241,815-143,287,014 , GRCh37.p13 chr8: 144,323,985-144,369,184 MINCR, GLI4, 1 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
    nsv6632568copy number variation1nstd224human GRCh37 chr8: 143,639,470-144,398,219 , GRCh38.p12 chr8: 142,558,109-143,316,049 CYP11B2, GLI4, 33 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
    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
    nsv6313759copy number variation1nstd102humanPathogenic GRCh37 chr8: 70,382,990-146,295,771 , GRCh38.p12 chr8: 69,470,755-145,070,385 LOC101927066, NCAPGP1, 1014 more genes
    nsv6313487copy number variation1nstd102humanPathogenic GRCh37 chr8: 130,863,093-146,295,771 , GRCh38.p12 chr8: 129,850,847-145,070,385 LOC105375784, CYP11B2, 253 more genes
    nsv6312709copy number variation2nstd102humanPathogenic GRCh37 chr8: 144,295,143-145,701,139 , GRCh38.p12 chr8: 143,213,268-144,475,756 MIR10400, BOP1, 83 more genes
    nsv6312626copy number variation3nstd102humanUncertain significance GRCh37 chr8: 143,822,561-145,743,168 , GRCh38.p12 chr8: 142,741,143-144,517,784 PYCR3, LOC101928902, 110 more genes
    nsv6137257copy number variation1nstd213human GRCh37 chr8: 144,290,000-144,500,001 , GRCh38.p12 chr8: 143,208,596-143,417,831 TOP1MT, RHPN1, 9 more genes
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