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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5521023copy number variation1nstd206human GRCh38 chr17: 44,189,898-44,190,074 , GRCh37.p13 chr17: 42,267,266-42,267,442 ATXN7L3, TMUB2
    nsv5293690copy number variation1nstd204human GRCh37.p13 chr17: 42,260,169-42,295,568 , GRCh38.p13 chr17: 44,182,801-44,218,200 UBTF, ATXN7L3, 4 more genes
    nsv5148892mobile element insertion1nstd203human GRCh38 chr17: 44,190,009-44,190,023 , GRCh37.p13 chr17: 42,267,377-42,267,391 ATXN7L3, TMUB2
    nsv5013737copy number variation1nstd200human GRCh38 chr17: 44,189,844-44,196,778 , GRCh37.p13 chr17: 42,267,212-42,274,146 TMUB2, ATXN7L3, 1 more genes
    nsv4864672copy number variation1nstd200human GRCh37 chr17: 42,267,213-42,274,146 , GRCh38.p12 chr17: 44,189,845-44,196,778 ATXN7L3, TMUB2, 1 more genes
    nsv4681862copy number variation1nstd102humanUncertain significance GRCh37 chr17: 42,105,175-42,430,244 , GRCh38.p12 chr17: 44,027,807-44,352,876 G6PC3, ATXN7L3, 21 more genes
    nsv4531994copy number variation1nstd166human GRCh37.p13 chr17: 42,274,395-42,274,594 , GRCh38.p12 chr17: 44,197,027-44,197,226 ATXN7L3-AS1, ATXN7L3
    nsv4370994copy number variation1nstd173human GRCh37 chr17: 42,204,597-42,399,013 , GRCh38.p12 chr17: 44,127,229-44,321,645 RNU6-453P, RN7SL507P, 15 more genes
    nsv4368311copy number variation1nstd173human GRCh37 chr17: 41,384,516-42,395,351 , GRCh38.p12 chr17: 43,307,154-44,317,983 , LOC105371789, 55 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
    nsv4268451copy number variation1nstd166human GRCh37.p13 chr17: 42,274,768-42,274,965 , GRCh38.p12 chr17: 44,197,400-44,197,597 ATXN7L3-AS1, ATXN7L3
    nsv4260333copy number variation1nstd166human GRCh37.p13 chr17: 42,274,000-42,280,000 , GRCh38.p12 chr17: 44,196,632-44,202,632 ATXN7L3-AS1, ATXN7L3
    nsv3966170copy number variation1nstd168human GRCh38 chr17: 44,197,341-44,213,368 , GRCh37.p13 chr17: 42,274,709-42,290,736 ATXN7L3-AS1, MIR6782, 2 more genes
    nsv3919609copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,648,246-42,839,745 , GRCh38 chr17: 43,570,878-44,762,377 , NCBI36 chr17: 39,003,772-40,195,271 SMCO4P1, LINC01180, 59 more genes
    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
    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
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