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Items: 1 to 20 of 160

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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
    nsv5358874translocation1nstd200human GRCh38 chr17: 42,661,918-42,661,918 , GRCh38 chr17: 42,661,830-42,661,830 , GRCh37.p13 chr17: 40,813,848-40,813,848 , GRCh37.p13 chr17: 40,813,936-40,813,936 TUBG2
    nsv5329081copy number variation1nstd204human GRCh37.p13 chr17: 40,816,468-40,820,030 , GRCh38.p13 chr17: 42,664,450-42,668,012 TUBG2, PLEKHH3
    nsv5293339copy number variation1nstd204human GRCh38.p13 chr17: 42,464,901-42,659,200 , GRCh37.p13 chr17: 40,616,919-40,811,218 ATP5MGP7, PTP4A2P1, 14 more genes
    nsv5290577copy number variation1nstd204human GRCh38.p13 chr17: 42,610,501-42,660,100 , GRCh37.p13 chr17: 40,762,519-40,812,118 HMGB3P27, TUBG1, 2 more genes
    nsv5287746copy number variation1nstd204human GRCh38.p13 chr17: 42,664,721-42,667,376 , GRCh37.p13 chr17: 40,816,739-40,819,394 PLEKHH3, TUBG2
    nsv5016443copy number variation1nstd200human GRCh38 chr17: 42,664,455-42,668,003 , GRCh37.p13 chr17: 40,816,473-40,820,021 PLEKHH3, TUBG2
    nsv5016442copy number variation1nstd200human GRCh38 chr17: 42,663,272-42,668,950 , GRCh37.p13 chr17: 40,815,290-40,820,968 TUBG2, PLEKHH3
    nsv4867039copy number variation1nstd200human GRCh37 chr17: 40,816,473-40,820,021 , GRCh38.p12 chr17: 42,664,455-42,668,003 PLEKHH3, TUBG2
    nsv4867038copy number variation1nstd200human GRCh37 chr17: 40,815,290-40,820,968 , GRCh38.p12 chr17: 42,663,272-42,668,950 PLEKHH3, TUBG2
    nsv4668105copy number variation1nstd186human GRCh37 chr17: 40,817,406-40,817,495 , GRCh38.p12 chr17: 42,665,388-42,665,477 TUBG2
    nsv4618884copy number variation1nstd183human GRCh37 chr17: 40,817,406-40,817,495 , GRCh38.p12 chr17: 42,665,388-42,665,477 TUBG2
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4271586copy number variation1nstd166human GRCh37.p13 chr17: 40,809,080-40,810,949 , GRCh38.p12 chr17: 42,657,062-42,658,931 TUBG2
    nsv4267541copy number variation1nstd166human GRCh37.p13 chr17: 40,763,000-40,812,000 , GRCh38.p12 chr17: 42,610,982-42,659,982 HMGB3P27, TUBG2, 2 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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