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Items: 1 to 20 of 236

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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
    nsv6877054copy number variation1nstd229human GRCh38 chr8: 142,769,230-142,847,719 , GRCh37.p13 chr8: 143,850,648-143,929,135 SLURP2, LYNX1, 3 more genes
    nsv6867364copy number variation1nstd229human GRCh38 chr8: 142,714,460-142,854,277 , GRCh37.p13 chr8: 143,813,537-143,935,693 SLURP1, LYPD2, 7 more genes
    nsv6863935copy number variation1nstd229human GRCh38 chr8: 142,670,749-142,846,341 , GRCh37.p13 chr8: 143,813,537-143,927,757 GML, SLURP1, 9 more genes
    nsv6862246copy number variation1nstd229human GRCh38 chr8: 142,749,201-142,796,900 , GRCh37.p13 chr8: 143,830,619-143,878,316 SLURP2, LY6D, 3 more genes
    nsv6860291copy number variation1nstd229human GRCh38 chr8: 142,691,701-142,842,600 , GRCh37.p13 chr8: 143,813,537-143,924,016 LNCOC1, LYPD2, 8 more genes
    nsv6859312copy number variation1nstd229human GRCh38 chr8: 142,765,140-142,769,754 , GRCh37.p13 chr8: 143,846,558-143,851,172 SLURP2, LYNX1, 1 more genes
    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
    nsv6632570copy number variation1nstd224human GRCh37 chr8: 143,854,600-143,927,993 , GRCh38.p12 chr8: 142,773,182-142,846,577 GML, LY6D, 2 more genes
    nsv6632569copy number variation1nstd224human GRCh37 chr8: 143,828,773-143,958,577 , GRCh38.p12 chr8: 142,747,355-142,877,161 CYP11B1, GML, 6 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
    nsv6419859copy number variation1nstd223human GRCh38 chr8: 142,714,458-142,854,276 , GRCh37.p13 chr8: 143,813,537-143,935,692 GML, LY6D, 7 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
    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
    nsv6312626copy number variation3nstd102humanUncertain significance GRCh37 chr8: 143,822,561-145,743,168 , GRCh38.p12 chr8: 142,741,143-144,517,784 PYCR3, LOC101928902, 110 more genes
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