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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7138293copy number variation1nstd232human GRCh37.p13 chr8: 145,152,035-145,152,131 , GRCh38.p12 chr8: 144,097,132-144,097,228 CYC1, SHARPIN
    nsv7072678inversion1nstd229human GRCh38 chr8: 144,103,096-144,103,212 , GRCh37.p13 chr8: 145,157,999-145,158,115 SHARPIN, MAF1
    nsv6876883copy number variation1nstd229human GRCh38 chr8: 144,025,878-144,405,710 , GRCh37.p13 chr8: 145,091,982-145,631,103 LOC101928902, MIR1234, 28 more genes
    nsv6873776copy number variation1nstd229human GRCh38 chr8: 143,662,901-144,626,400 , GRCh37.p13 chr8: 145,146,063-145,851,785 LRRC14, SCX, 67 more genes
    nsv6871471copy number variation1nstd229human GRCh38 chr8: 144,097,001-144,100,100 , GRCh37.p13 chr8: 145,151,904-145,155,003 SHARPIN, CYC1
    nsv6866250copy number variation1nstd229human GRCh38 chr8: 143,771,901-144,562,100 , GRCh37.p13 chr8: 145,146,063-145,787,484 MIR939, MIR10400, 58 more genes
    nsv6863828copy number variation1nstd229human GRCh38 chr8: 144,096,763-144,096,791 , GRCh37.p13 chr8: 145,151,666-145,151,694 CYC1, SHARPIN
    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
    nsv6558782inversion1nstd223human GRCh38 chr8: 143,001,224-145,028,420 , GRCh37.p13 chr8: 144,082,641-146,253,806 ZFP41, LY6H, 118 more genes
    nsv6430368copy number variation1nstd223human GRCh38 chr8: 144,023,890-144,301,209 , GRCh37.p13 chr8: 145,146,063-145,285,644 CYC1, GPAA1, 16 more genes
    nsv6430241copy number variation1nstd223human GRCh38 chr8: 143,844,521-144,567,758 , GRCh37.p13 chr8: 145,146,063-145,793,142 MFSD3, SLC39A4, 51 more genes
    nsv6417121copy number variation1nstd223human GRCh38 chr8: 143,683,447-144,365,810 , GRCh37.p13 chr8|NW_003315923.1: 22,092-429,806 , GRCh37.p13 chr8: 144,765,617-145,589,470 EPPK1, PARP10, 42 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
    nsv6136021copy number variation1nstd213human GRCh37 chr8: 144,920,000-145,290,001 , GRCh38.p12 chr8: 143,837,828-144,235,098 GPAA1, HGH1, 19 more genes
    nsv5381643copy number variation1nstd102humanUncertain significance GRCh37 chr8: 145,047,561-145,701,149 , GRCh38.p12 chr8: 143,973,393-144,475,766 ZFTRAF1, DGAT1, 40 more genes
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