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Items: 1 to 20 of 125

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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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 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
    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
    nsv3161480copy number variation2nstd151human GRCh37 chr17: 40,913,849-40,914,875 , GRCh38.p12 chr17: 42,761,831-42,762,857 RAMP2
    esv4010331copy number variation1estd233human GRCh37 chr17: 40,804,000-41,398,000 , GRCh38.p12 chr17: 42,651,982-43,320,637 , AOC2, 41 more genes
    nsv2766373copy number variation1nstd130human GRCh37 chr17: 39,883,350-41,512,322 , GRCh38.p12 chr17: 41,727,098-43,434,954 , ACLY, 91 more genes
    nsv1874817short tandem repeat4nstd128human GRCh37 chr17: 40,911,273-40,911,287 , GRCh38.p12 chr17: 42,759,255-42,759,269 RAMP2-AS1, RAMP2
    nsv1146669inversion1nstd107human GRCh37 chr17: 36,350,713-45,671,345 , GRCh38.p12 chr17: 38,545,381-47,593,979 , ACLY, 444 more genes
    nsv1141883inversion1nstd106human GRCh37 chr17: 5,045,567-58,288,633 , GRCh38.p12 chr17: 5,142,272-60,211,272 , AK4P1, 1655 more genes
    esv3814981copy number variation1estd192human GRCh37 chr17: 31,815,863-49,448,152 , GRCh38.p12 chr17: 33,488,845-51,370,791 , LOC101929777, 757 more genes
    esv3815514tandem duplication1estd192human GRCh37 chr17: 33,138,815-78,400,182 , GRCh38.p12 chr17: 34,811,796-80,426,382 , SCRN2, 1365 more genes
    esv3815563tandem duplication1estd192human GRCh37 chr17: 30,934,818-54,638,435 , GRCh38.p12 chr17: 32,607,800-56,561,074 , CCL14, 800 more genes
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