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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147603copy number variation1nstd232human GRCh37.p13 chr17: 38,146,179-38,146,342 , GRCh38.p12 chr17: 39,989,926-39,990,089 PSMD3
    nsv7095150copy number variation1nstd102humanUncertain significance GRCh37 chr17: 37,821,613-38,458,253 , GRCh38.p12 chr17: 39,665,360-40,302,001 ZPBP2, MED24, 28 more genes
    nsv7073998inversion1nstd229human GRCh38 chr17: 32,918,710-41,148,753 , GRCh37.p13 chr17: 31,245,728-39,305,005 LOC105371750, C17orf78, 298 more genes
    nsv6991593copy number variation1nstd229human GRCh38 chr17: 39,985,289-39,985,762 , GRCh37.p13 chr17: 38,141,542-38,142,015 PSMD3
    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
    nsv6503362copy number variation1nstd223human GRCh38 chr17: 39,998,423-39,998,948 , GRCh37.p13 chr17: 38,154,676-38,155,201 PSMD3
    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
    nsv5978767insertion1nstd209human GRCh38 chr17: 39,992,024-39,992,024 , GRCh37.p13 chr17: 38,148,277-38,148,277 PSMD3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5531677copy number variation1nstd206human GRCh38 chr17: 39,964,379-39,998,368 , GRCh37.p13 chr17: 38,120,632-38,154,621 PSMD3, GSDMA
    nsv5519011copy number variation1nstd206human GRCh38 chr17: 39,916,896-39,986,562 , GRCh37.p13 chr17: 38,073,149-38,142,815 , PSMD3, 4 more genes
    nsv5341813translocation1nstd200human GRCh37 chr17: 38,142,038-38,142,038 , GRCh37 chr17: 38,141,727-38,141,727 , GRCh38.p12 chr17: 39,985,474-39,985,474 , GRCh38.p12 chr17: 39,985,785-39,985,785 PSMD3
    nsv5283669copy number variation1nstd204human GRCh38.p13 chr17: 39,851,001-40,379,500 , GRCh37.p13 chr17: 38,007,254-38,535,752 , CASC3, 27 more genes
    nsv5013687copy number variation1nstd200human GRCh38 chr17: 39,985,289-39,985,766 , GRCh37.p13 chr17: 38,141,542-38,142,019 PSMD3
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4256824copy number variation1nstd166human GRCh37.p13 chr17: 38,141,727-38,142,038 , GRCh38.p12 chr17: 39,985,474-39,985,785 PSMD3
    nsv4252628copy number variation1nstd166human GRCh37.p13 chr17: 38,141,542-38,142,019 , GRCh38.p12 chr17: 39,985,289-39,985,766 PSMD3
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
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