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Items: 1 to 20 of 198

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5523645copy number variation1nstd206human GRCh38 chr17: 76,006,457-76,016,203 , GRCh37.p13 chr17: 74,002,538-74,012,284 TEN1-CDK3, EVPL, 1 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5152601mobile element insertion1nstd203human GRCh38 chr17: 75,992,840-75,992,861 , GRCh37.p13 chr17: 73,988,921-73,988,942 TEN1, TEN1-CDK3
    nsv5016727copy number variation1nstd200human GRCh38 chr17: 76,004,456-76,004,563 , GRCh37.p13 chr17: 74,000,537-74,000,644 CDK3, TEN1-CDK3
    nsv5016726copy number variation1nstd200human GRCh38 chr17: 75,987,015-75,994,265 , GRCh37.p13 chr17: 73,983,096-73,990,346 TEN1-CDK3, TEN1
    nsv5016725copy number variation1nstd200human GRCh38 chr17: 75,981,477-75,985,722 , GRCh37.p13 chr17: 73,977,558-73,981,803 TEN1-CDK3, TEN1
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4513517mobile element insertion1nstd166human GRCh37.p13 chr17: 73,978,180-73,978,180 , GRCh38.p12 chr17: 75,982,099-75,982,099 TEN1-CDK3, TEN1
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4271331copy number variation1nstd166human GRCh37.p13 chr17: 73,981,843-73,990,746 , GRCh38.p12 chr17: 75,985,762-75,994,665 TEN1-CDK3, TEN1
    nsv4270319copy number variation1nstd166human GRCh37.p13 chr17: 73,977,247-73,980,535 , GRCh38.p12 chr17: 75,981,166-75,984,454 TEN1, TEN1-CDK3
    nsv3972399copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942 AANAT, ACOX1, 243 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 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
    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
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 RPL38, RNF157-AS1, 428 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
    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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