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Items: 1 to 20 of 21

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095156copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,894-41,063,443 , GRCh38.p12 chr17: 42,900,877-42,911,426 G6PC1
    nsv5672880copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,055,938-41,063,453 , GRCh38.p12 chr17: 42,903,921-42,911,436 G6PC1
    nsv7094974copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,894-41,059,665 , GRCh38.p12 chr17: 42,900,877-42,907,648 G6PC1
    nsv4681486copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,817-41,056,246 , GRCh38.p12 chr17: 42,900,800-42,904,229 G6PC1
    nsv7095155copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,052,894-41,056,246 , GRCh38.p12 chr17: 42,900,877-42,904,229 G6PC1
    nsv7095157copy number variation1nstd102humanPathogenic GRCh37 chr17: 41,055,928-41,056,246 , GRCh38.p12 chr17: 42,903,911-42,904,229 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
    nsv7095158copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 41,061,310-41,061,445 , GRCh38.p12 chr17: 42,909,293-42,909,428 G6PC1
    nsv7094887copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,059,520-41,063,443 , GRCh38.p12 chr17: 42,907,503-42,911,426 G6PC1
    nsv7095154copy number variation1nstd102humanUncertain significance GRCh37 chr17: 41,052,894-41,053,143 , GRCh38.p12 chr17: 42,900,877-42,901,126 G6PC1
    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 G6PC1, PRPSAP1, 1350 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 G6PC1, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 G6PC1, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 G6PC1, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 G6PC1, SMURF2, 2366 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 G6PC1, LOC105371922, 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 G6PC1, RNU6-131P, 1075 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 G6PC1, PLEKHH3, 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 G6PC1, IFI35, 345 more genes
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