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Items: 1 to 20 of 206

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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
    nsv7066364inversion1nstd229human GRCh38 chr8: 137,405,728-137,405,764 , GRCh37.p13 chr8: 138,417,971-138,418,007 LOC101927915
    nsv6878085copy number variation1nstd229human GRCh38 chr8: 137,137,015-137,705,256 , GRCh37.p13 chr8: 138,149,258-138,717,499 LOC107986905, ZYXP1, 2 more genes
    nsv6877164copy number variation1nstd229human GRCh38 chr8: 137,403,006-137,405,632 , GRCh37.p13 chr8: 138,415,249-138,417,875 LOC101927915
    nsv6871427copy number variation1nstd229human GRCh38 chr8: 137,236,501-137,427,000 , GRCh37.p13 chr8: 138,248,744-138,439,243 LOC101927915, ZYXP1
    nsv6869275copy number variation1nstd229human GRCh38 chr8: 136,983,405-137,679,700 , GRCh37.p13 chr8: 137,995,648-138,691,943 RNU6-144P, LOC107986905, 2 more genes
    nsv6863500copy number variation1nstd229human GRCh38 chr8: 137,371,131-137,437,174 , GRCh37.p13 chr8: 138,383,374-138,449,417 ZYXP1, LOC101927915
    nsv6862294copy number variation1nstd229human GRCh38 chr8: 137,410,361-137,410,441 , GRCh37.p13 chr8: 138,422,604-138,422,684 LOC101927915
    nsv6862008copy number variation1nstd229human GRCh38 chr8: 137,391,076-137,413,727 , GRCh37.p13 chr8: 138,403,319-138,425,970 LOC101927915
    nsv6858840copy number variation1nstd229human GRCh38 chr8: 135,810,557-138,287,683 , GRCh37.p13 chr8: 136,822,800-139,299,926 LOC107986978, RNU6-144P, 10 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
    nsv6435038copy number variation1nstd223human GRCh38 chr8: 137,410,359-137,410,441 , GRCh37.p13 chr8: 138,422,602-138,422,684 LOC101927915
    nsv6434930copy number variation1nstd223human GRCh38 chr8: 137,402,301-137,404,200 , GRCh37.p13 chr8: 138,414,544-138,416,443 LOC101927915
    nsv6433457copy number variation1nstd223human GRCh38 chr8: 136,656,670-137,924,604 , GRCh37.p13 chr8: 137,668,913-138,936,847 LOC401478, LOC100129367, 6 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
    nsv6294848mobile element insertion1nstd186human GRCh37 chr8: 138,416,660-138,416,711 , GRCh38.p12 chr8: 137,404,417-137,404,468 LOC101927915
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