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Items: 1 to 20 of 143

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5887166copy number variation1nstd209human GRCh38 chr17: 42,868,187-42,874,194 , GRCh37.p13 chr17: 41,020,204-41,026,211 LINC00671, AOC4P
    nsv5879763copy number variation2nstd209human GRCh38 chr17: 42,853,445-42,869,919 , GRCh37.p13 chr17: 41,005,462-41,021,936 AOC3, AOC4P
    nsv5871553copy number variation2nstd209human GRCh38 chr17: 42,860,968-42,868,108 , GRCh37.p13 chr17: 41,012,985-41,020,125 AOC4P
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5016449copy number variation1nstd200human GRCh38 chr17: 42,852,936-42,868,817 , GRCh37.p13 chr17: 41,004,953-41,020,834 AOC3, AOC4P
    nsv4858853copy number variation1nstd200human GRCh37 chr17: 41,004,937-41,020,855 , GRCh38.p12 chr17: 42,852,920-42,868,838 AOC3, AOC4P
    nsv4622584copy number variation1nstd183human GRCh37 chr17: 41,008,651-41,023,580 , GRCh38.p12 chr17: 42,856,634-42,871,563 AOC4P, AOC3
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4270005copy number variation1nstd166human GRCh37.p13 chr17: 41,004,000-41,019,300 , GRCh38.p12 chr17: 42,851,983-42,867,283 AOC4P, AOC3
    nsv4258631copy number variation1nstd166human GRCh37.p13 chr17: 41,010,977-41,033,734 , GRCh38.p12 chr17: 42,858,960-42,881,717 AOC4P, LINC00671
    nsv4253475copy number variation1nstd166human GRCh37.p13 chr17: 40,999,800-41,069,100 , GRCh38.p12 chr17: 42,847,783-42,917,083 AOC2, G6PC1, 4 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
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