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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv7066656inversion1nstd229human GRCh38 chr17: 40,822,205-41,582,529 , GRCh37.p13 chr17: 38,978,457-39,738,781 LOC105371777, KRT10, 69 more genes
    nsv6995384copy number variation1nstd229human GRCh38 chr17: 40,954,453-40,984,707 , GRCh37.p13 chr17: 39,110,705-39,140,959 KRT39, LOC107985072, 1 more genes
    nsv6992218copy number variation1nstd229human GRCh38 chr17: 40,934,745-41,023,836 , GRCh37.p13 chr17: 39,090,997-39,180,088 KRT40, KRTAP3-1, 6 more genes
    nsv6989996copy number variation1nstd229human GRCh38 chr17: 40,978,598-40,978,649 , GRCh37.p13 chr17: 39,134,850-39,134,901 LOC107985072, KRT40
    nsv6985729copy number variation1nstd229human GRCh38 chr17: 40,909,717-40,979,612 , GRCh37.p13 chr17: 39,065,969-39,135,864 KRT23, KRT39, 3 more genes
    nsv6984984copy number variation1nstd229human GRCh38 chr17: 38,377,708-42,855,253 , GRCh37.p13 chr17: 36,701,616-41,007,270 ZNF385C, AOC2, 248 more genes
    nsv6982861copy number variation1nstd229human GRCh38 chr17: 38,291,672-47,498,259 , GRCh37.p13 chr17: 36,510,266-45,575,625 KRT20, PLEKHH3, 442 more genes
    nsv6980804copy number variation1nstd229human GRCh38 chr17: 40,949,294-41,074,654 , GRCh37.p13 chr17: 39,105,546-39,230,906 KRTAP3-3, KRTAP3-1, 14 more genes
    nsv6513274copy number variation1nstd223human GRCh38 chr17: 40,985,213-40,985,648 , GRCh37.p13 chr17: 39,141,465-39,141,900 KRT40
    nsv6509451copy number variation1nstd223human GRCh38 chr17: 40,934,745-41,023,836 , GRCh37.p13 chr17: 39,090,997-39,180,088 KRT23, KRTAP3-2, 6 more genes
    nsv6193307copy number variation1nstd214human GRCh38 chr17: 40,978,598-40,978,648 , GRCh37.p13 chr17: 39,134,850-39,134,900 KRT40, LOC107985072
    nsv6133056copy number variation1nstd213human GRCh37 chr17: 36,400,000-39,740,001 , GRCh38.p12 chr17: 38,545,381-41,583,749 CACNB1, CDC6, 176 more genes
    nsv5934394copy number variation1nstd209human GRCh38 chr17: 40,978,598-40,978,648 , GRCh37.p13 chr17: 39,134,850-39,134,900 LOC107985072, KRT40
    nsv5590520copy number variation1nstd207human GRCh38 chr17: 40,978,598-40,978,648 , GRCh37.p13 chr17: 39,134,850-39,134,900 KRT40, LOC107985072
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5526860copy number variation1nstd206human GRCh38 chr17: 40,978,598-40,978,649 , GRCh37.p13 chr17: 39,134,850-39,134,901 KRT40, LOC107985072
    nsv5518631copy number variation1nstd206human GRCh38 chr17: 40,902,081-41,114,453 , GRCh37.p13 chr17: 39,058,333-39,270,705 KRTAP2-3, LOC105371777, 20 more genes
    nsv5324143copy number variation1nstd204human GRCh37.p13 chr17: 39,132,129-39,135,100 , GRCh38.p13 chr17: 40,975,877-40,978,848 LOC107985072, KRT40
    nsv5016353copy number variation1nstd200human GRCh38 chr17: 40,985,191-40,985,845 , GRCh37.p13 chr17: 39,141,443-39,142,097 KRT40
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