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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938206copy number variation1nstd209human GRCh38 chr17: 42,904,920-42,905,352 , GRCh37.p13 chr17: 41,056,937-41,057,369 G6PC1
    nsv5673118copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,059,530-41,059,655 , GRCh38.p12 chr17: 42,907,513-42,907,638 G6PC1
    nsv5673099copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,053,048-41,053,049 , GRCh38 chr17: 42,901,031-42,901,032 G6PC1
    nsv5672880copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,055,938-41,063,453 , GRCh38.p12 chr17: 42,903,921-42,911,436 G6PC1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5526220copy number variation1nstd206human GRCh38 chr17: 42,904,922-42,905,353 , GRCh37.p13 chr17: 41,056,939-41,057,370 G6PC1
    nsv5203218mobile element deletion1nstd204human GRCh38.p13 chr17: 42,914,576-42,914,929 , GRCh37.p13 chr17: 41,066,593-41,066,946 G6PC1
    nsv4907344mobile element deletion1nstd200human GRCh38 chr17: 42,914,606-42,914,900 , GRCh37.p13 chr17: 41,066,623-41,066,917 G6PC1
    nsv4769500mobile element deletion1nstd200human GRCh37 chr17: 41,066,623-41,066,917 , GRCh38.p12 chr17: 42,914,606-42,914,900 G6PC1
    nsv4681486copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,817-41,056,246 , GRCh38.p12 chr17: 42,900,800-42,904,229 G6PC1
    nsv4623252copy number variation1nstd183human GRCh37 chr17: 41,058,485-41,098,754 , GRCh38.p12 chr17: 42,906,468-42,946,737 RNY4P2, G6PC1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    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
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