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Items: 1 to 20 of 138

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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
    nsv5341713translocation1nstd200human GRCh37 chr17: 38,850,381-38,850,381 , GRCh37 chr17: 38,850,476-38,850,476 , GRCh38.p12 chr17: 40,694,129-40,694,129 , GRCh38.p12 chr17: 40,694,224-40,694,224 KRT24, LOC105371775
    nsv5013693copy number variation1nstd200human GRCh38 chr17: 40,682,814-40,699,207 , GRCh37.p13 chr17: 38,839,066-38,855,459 LOC105371775, KRT24
    nsv4864649copy number variation1nstd200human GRCh37 chr17: 38,839,066-38,855,459 , GRCh38.p12 chr17: 40,682,814-40,699,207 LOC105371775, KRT24
    nsv4679355copy number variation1nstd189human GRCh37.p13 chr17: 38,659,900-39,414,647 , GRCh38.p12 chr17: 40,503,648-41,258,395 , CCR7, 54 more genes
    nsv4365890copy number variation1nstd173human GRCh37 chr17: 38,846,470-38,880,294 , GRCh38.p12 chr17: 40,690,218-40,724,042 LOC105371775, KRT24, 1 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
    nsv4265791copy number variation1nstd166human GRCh37.p13 chr17: 38,849,503-38,849,707 , GRCh38.p12 chr17: 40,693,251-40,693,455 LOC105371775, KRT24
    nsv4253252copy number variation1nstd166human GRCh37.p13 chr17: 38,839,144-38,855,417 , GRCh38.p12 chr17: 40,682,892-40,699,165 LOC105371775, KRT24
    nsv3948881copy number variation1nstd167human GRCh37 chr17: 38,857,996-38,858,028 , GRCh38.p12 chr17: 40,701,744-40,701,776 KRT24
    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
    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
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3166943copy number variation1nstd151human GRCh37 chr17: 38,854,787-38,856,640 , GRCh38.p12 chr17: 40,698,535-40,700,388 KRT24
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