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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
    nsv3912159copy number variation1nstd102humanUncertain significance GRCh38 chr17: 39,876,786-40,048,205 , NCBI36 chr17: 35,286,565-35,457,984 , GRCh37 chr17: 38,033,039-38,204,458 PSMD3, MED24, 8 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3911344copy number variation1nstd102humanPathogenic GRCh37 chr17: 37,356,126-43,706,945 , NCBI36 chr17: 34,609,652-41,062,728 , GRCh38 chr17: 39,199,873-45,629,579 IFI35, RND2, 345 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
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