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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970348insertion1nstd209human GRCh38 chr17: 57,970,178-57,970,178 , GRCh37.p13 chr17: 56,047,539-56,047,539 VEZF1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5358991translocation1nstd200human GRCh38 chr17: 57,983,395-57,983,395 , GRCh38 chr17: 57,988,077-57,988,077 , GRCh37.p13 chr17: 56,065,438-56,065,438 , GRCh37.p13 chr17: 56,060,756-56,060,756 LOC101929185, VEZF1
    nsv5334035translocation1nstd200human GRCh37 chr17: 56,060,756-56,060,756 , GRCh37 chr17: 56,065,438-56,065,438 , GRCh38.p12 chr17: 57,983,395-57,983,395 , GRCh38.p12 chr17: 57,988,077-57,988,077 VEZF1, LOC101929185
    nsv5158521mobile element insertion1nstd203human GRCh38 chr17: 57,970,167-57,970,195 , GRCh37.p13 chr17: 56,047,528-56,047,556 VEZF1
    nsv5151726mobile element insertion1nstd203human GRCh38 chr17: 57,970,178-57,970,195 , GRCh37.p13 chr17: 56,047,539-56,047,556 VEZF1
    nsv5148382mobile element insertion1nstd203human GRCh38 chr17: 57,970,195-57,970,205 , GRCh37.p13 chr17: 56,047,556-56,047,566 VEZF1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4253577copy number variation1nstd166human GRCh37.p13 chr17: 56,027,328-56,051,269 , GRCh38.p12 chr17: 57,949,967-57,973,908 CUEDC1, VEZF1
    nsv3920623copy number variation1nstd102humanPathogenic GRCh37 chr17: 54,760,866-56,162,300 , NCBI36 chr17: 52,115,865-53,517,299 , GRCh38 chr17: 56,683,505-58,084,939 C17orf67, CUEDC1, 28 more genes
    nsv3917224copy number variation1nstd102humanPathogenic GRCh38 chr17: 56,958,745-58,171,125 , NCBI36 chr17: 52,391,105-53,603,485 , GRCh37 chr17: 55,036,106-56,248,486 MRPS23, MSX2P1, 24 more genes
    nsv3914957copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,496,167-57,812,825 , GRCh38 chr17: 57,418,806-59,735,464 , NCBI36 chr17: 52,851,166-55,167,607 CLTC, LOC101927557, 67 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
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906711copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 55,916,829-56,770,618 , GRCh38.p12 chr17: 57,839,468-58,693,257 LPO, MPO, 34 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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