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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7098162copy number variation1nstd102humanUncertain significance GRCh37 chr8: 139,601,496-141,468,663 , GRCh38.p12 chr8: 138,589,253-140,458,564 LOC100421256, KCNK9, 6 more genes
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv6873545copy number variation1nstd229human GRCh38 chr8: 139,880,373-139,921,696 , GRCh37.p13 chr8: 140,892,617-140,933,940 LOC105375781, TRAPPC9
    nsv6872045copy number variation1nstd229human GRCh38 chr8: 138,206,201-140,157,100 , GRCh37.p13 chr8: 139,218,444-141,167,199 TRAPPC9, KCNK9, 6 more genes
    nsv6869739copy number variation1nstd229human GRCh38 chr8: 139,907,286-140,046,330 , GRCh37.p13 chr8: 140,919,530-141,056,427 LOC105375781, TRAPPC9, 1 more genes
    nsv6867372copy number variation1nstd229human GRCh38 chr8: 139,600,301-139,959,200 , GRCh37.p13 chr8: 140,612,544-140,971,633 LOC105375781, TRAPPC9, 2 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
    nsv6632677copy number variation1nstd224human GRCh37 chr8: 140,170,480-141,449,601 , GRCh38.p12 chr8: 139,158,237-140,439,502 KCNK9, TRAPPC9, 5 more genes
    nsv6430707copy number variation1nstd223human GRCh38 chr8: 139,600,401-140,174,600 , GRCh37.p13 chr8: 140,612,644-141,184,699 LOC105375781, TRAPPC9, 4 more genes
    nsv6428327copy number variation1nstd223human GRCh38 chr8: 139,916,991-139,919,239 , GRCh37.p13 chr8: 140,929,235-140,931,483 TRAPPC9, LOC105375781
    nsv6424718copy number variation1nstd223human GRCh38 chr8: 139,704,201-140,110,200 , GRCh37.p13 chr8: 140,716,444-141,120,299 TRAPPC9, LOC100421256, 3 more genes
    nsv6420403copy number variation1nstd223human GRCh38 chr8: 139,902,201-139,990,900 , GRCh37.p13 chr8: 140,914,445-141,001,110 LOC105375781, TRAPPC9
    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
    nsv6290267copy number variation1nstd102humanUncertain significance GRCh37 chr8: 139,692,209-141,412,715 , GRCh38.p12 chr8: 138,679,966-140,402,616 TRAPPC9, KCNK9, 6 more genes
    nsv6290242copy number variation1nstd102humanUncertain significance GRCh37 chr8: 128,878,931-141,662,233 , GRCh38.p12 chr8: 127,866,685-140,652,134 LINC02055, LOC101927798, 100 more genes
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