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Items: 1 to 20 of 218

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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
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7066490inversion1nstd229human GRCh38 chr8: 140,511,338-140,515,829 , GRCh37.p13 chr8: 141,521,437-141,525,928 CHRAC1
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv6876937copy number variation1nstd229human GRCh38 chr8: 140,455,722-140,543,806 , GRCh37.p13 chr8: 141,465,821-141,553,905 AGO2, TRAPPC9, 2 more genes
    nsv6873068copy number variation1nstd229human GRCh38 chr8: 140,429,472-140,526,693 , GRCh37.p13 chr8: 141,439,571-141,536,792 AGO2, CHRAC1, 2 more genes
    nsv6870021copy number variation1nstd229human GRCh38 chr8: 140,442,301-140,514,200 , GRCh37.p13 chr8: 141,452,400-141,524,299 CHRAC1, LOC105375782, 1 more genes
    nsv6866481copy number variation1nstd229human GRCh38 chr8: 140,514,800-140,518,604 , GRCh37.p13 chr8: 141,524,899-141,528,703 CHRAC1, AGO2
    nsv6862141copy number variation1nstd229human GRCh38 chr8: 140,504,758-140,509,475 , GRCh37.p13 chr8: 141,514,857-141,519,574 CHRAC1
    nsv6861891copy number variation1nstd229human GRCh38 chr8: 140,213,487-140,517,801 , GRCh37.p13 chr8: 141,223,586-141,527,900 TRAPPC9, CHRAC1, 2 more genes
    nsv6637760copy number variation1nstd102humanUncertain significance GRCh37 chr8: 141,352,715-141,656,635 , GRCh38.p12 chr8: 140,342,616-140,646,536 LOC107986982, AGO2, 3 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
    nsv6434825copy number variation1nstd223human GRCh38 chr8: 140,508,601-140,513,300 , GRCh37.p13 chr8: 141,518,700-141,523,399 CHRAC1
    nsv6430966copy number variation1nstd223human GRCh38 chr8: 140,429,472-140,526,693 , GRCh37.p13 chr8: 141,439,571-141,536,792 CHRAC1, AGO2, 2 more genes
    nsv6423267copy number variation1nstd223human GRCh38 chr8: 140,419,094-141,917,651 , GRCh37.p13 chr8: 141,429,193-142,999,012 RNA5SP278, LOC105375782, 24 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
    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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