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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6876566copy number variation1nstd229human GRCh38 chr8: 142,649,793-142,653,331 , GRCh37.p13 chr8|NW_003871066.2: 19,926-23,464 , GRCh37.p13 chr8: 143,731,177-143,734,715 JRK
    nsv6874843copy number variation1nstd229human GRCh38 chr8: 142,659,221-142,676,187 , GRCh37.p13 chr8|NW_003871066.2: 29,354-46,320 , GRCh37.p13 chr8: 143,740,633-143,757,605 JRK, PSCA
    nsv6873588copy number variation1nstd229human GRCh38 chr8: 142,648,080-142,657,745 , GRCh37.p13 chr8: 143,729,464-143,739,159 , GRCh37.p13 chr8|NW_003871066.2: 18,213-27,878 JRK
    nsv6871400copy number variation1nstd229human GRCh38 chr8: 142,558,701-142,684,700 , GRCh37.p13 chr8: 143,640,062-143,711,228 JRK, ARC, 3 more genes
    nsv6867704copy number variation1nstd229human GRCh38 chr8: 142,654,523-142,661,054 , GRCh37.p13 chr8|NW_003871066.2: 24,656-31,187 , GRCh37.p13 chr8: 143,735,907-143,742,466 JRK
    nsv6867341copy number variation1nstd229human GRCh38 chr8: 142,660,029-142,662,400 , GRCh37.p13 chr8|NW_003871066.2: 30,162-32,533 , GRCh37.p13 chr8: 143,741,441-143,743,812 JRK
    nsv6862530copy number variation1nstd229human GRCh38 chr8: 142,644,806-142,649,907 , GRCh37.p13 chr8: 143,726,190-143,731,291 , GRCh37.p13 chr8|NW_003871066.2: 14,939-20,040 JRK
    nsv6861781copy number variation1nstd229human GRCh38 chr8: 142,655,617-142,658,311 , GRCh37.p13 chr8: 143,737,008-143,739,725 , GRCh37.p13 chr8|NW_003871066.2: 25,750-28,444 JRK
    nsv6637631copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,836,592-144,175,046 , GRCh38.p12 chr8: 141,755,231-143,093,629 CYP11B1, LOC105375792, 33 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
    nsv6632568copy number variation1nstd224human GRCh37 chr8: 143,639,470-144,398,219 , GRCh38.p12 chr8: 142,558,109-143,316,049 CYP11B2, GLI4, 33 more genes
    nsv6417526copy number variation1nstd223human GRCh38 chr8: 142,256,520-142,935,362 , GRCh37.p13 chr8: 143,337,881-144,016,778 ZNHIT1P1, MROH4P, 19 more genes
    nsv6416074copy number variation1nstd223human GRCh38 chr8: 142,626,828-142,660,045 , GRCh37.p13 chr8: 143,711,229-143,741,457 , GRCh37.p13 chr8|NW_003871066.2: 1-30,178 JRK, LOC101928087
    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
    nsv6301253copy number variation1nstd186human GRCh37 chr8: 143,750,952-143,751,126 , GRCh38.p12 chr8: 142,669,534-142,669,708 JRK, PSCA
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