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Items: 1 to 20 of 1186

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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
    nsv7146432insertion1nstd232human GRCh37.p13 chr8: 139,818,401-139,818,401 , GRCh38.p12 chr8: 138,806,158-138,806,158 COL22A1
    nsv7141967insertion1nstd232human GRCh37.p13 chr8: 139,818,276-139,818,276 , GRCh38.p12 chr8: 138,806,033-138,806,033 COL22A1
    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
    nsv7077693inversion1nstd229human GRCh38 chr8: 138,870,643-138,882,445 , GRCh37.p13 chr8: 139,882,886-139,894,688 COL22A1
    nsv7076791inversion1nstd229human GRCh38 chr8: 138,651,993-138,657,082 , GRCh37.p13 chr8: 139,664,236-139,669,325 COL22A1
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7070184inversion1nstd229human GRCh38 chr8: 138,894,261-138,899,031 , GRCh37.p13 chr8: 139,906,504-139,911,274 COL22A1
    nsv7068866inversion1nstd229human GRCh38 chr8: 138,727,360-138,728,903 , GRCh37.p13 chr8: 139,739,603-139,741,146 COL22A1
    nsv7065870inversion1nstd229human GRCh38 chr8: 138,819,652-138,826,956 , GRCh37.p13 chr8: 139,831,895-139,839,199 COL22A1
    nsv7063227inversion1nstd229human GRCh38 chr8: 138,815,484-138,826,291 , GRCh37.p13 chr8: 139,827,727-139,838,534 COL22A1
    nsv6878063copy number variation1nstd229human GRCh38 chr8: 138,888,941-138,890,257 , GRCh37.p13 chr8: 139,901,184-139,902,500 COL22A1
    nsv6877400copy number variation1nstd229human GRCh38 chr8: 138,674,297-138,676,547 , GRCh37.p13 chr8: 139,686,540-139,688,790 COL22A1
    nsv6876792copy number variation1nstd229human GRCh38 chr8: 138,814,422-138,814,449 , GRCh37.p13 chr8: 139,826,665-139,826,692 COL22A1
    nsv6876505copy number variation1nstd229human GRCh38 chr8: 138,711,822-138,715,368 , GRCh37.p13 chr8: 139,724,065-139,727,611 COL22A1
    nsv6875590copy number variation1nstd229human GRCh38 chr8: 138,884,942-138,889,978 , GRCh37.p13 chr8: 139,897,185-139,902,221 COL22A1
    nsv6874540copy number variation1nstd229human GRCh38 chr8: 138,597,626-138,615,584 , GRCh37.p13 chr8: 139,609,869-139,627,827 COL22A1
    nsv6873940copy number variation1nstd229human GRCh38 chr8: 138,766,171-138,770,778 , GRCh37.p13 chr8: 139,778,414-139,783,021 COL22A1
    nsv6872377copy number variation1nstd229human GRCh38 chr8: 138,903,799-138,904,040 , GRCh37.p13 chr8: 139,916,042-139,916,283 COL22A1
    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

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