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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5931218copy number variation1nstd209human GRCh38 chr17: 4,805,157-4,805,450 , GRCh37.p13 chr17: 4,708,452-4,708,745 PLD2
    nsv5584774copy number variation1nstd207human GRCh38 chr17: 4,820,133-4,820,456 , GRCh37.p13 chr17: 4,723,428-4,723,751 PLD2
    nsv5526090copy number variation1nstd206human GRCh38 chr17: 4,820,876-4,821,201 , GRCh37.p13 chr17: 4,724,171-4,724,496 PLD2
    nsv5518565copy number variation1nstd206human GRCh38 chr17: 4,812,581-4,820,790 , GRCh37.p13 chr17: 4,715,876-4,724,085 PLD2
    nsv5515629copy number variation1nstd206human GRCh38 chr17: 4,798,328-4,821,338 , GRCh37.p13 chr17: 4,701,623-4,724,633 PLD2, PSMB6
    nsv5358585translocation1nstd200human GRCh38 chr17: 4,821,376-4,821,376 , GRCh38 chr17: 4,822,657-4,822,657 , GRCh37.p13 chr17: 4,725,952-4,725,952 , GRCh37.p13 chr17: 4,724,671-4,724,671 PLD2
    nsv5339820translocation1nstd200human GRCh37 chr17: 4,724,671-4,724,671 , GRCh37 chr17: 4,725,952-4,725,952 , GRCh38.p12 chr17: 4,821,376-4,821,376 , GRCh38.p12 chr17: 4,822,657-4,822,657 PLD2
    nsv5320279copy number variation1nstd204human GRCh38.p13 chr17: 4,820,094-4,820,632 , GRCh37.p13 chr17: 4,723,389-4,723,927 PLD2
    nsv5299082copy number variation1nstd204human GRCh37.p13 chr17: 4,627,696-4,727,995 , GRCh38.p13 chr17: 4,724,401-4,824,700 PLD2, PSMB6, 6 more genes
    nsv4864479copy number variation1nstd200human GRCh37 chr17: 4,687,640-4,824,332 , GRCh38.p12 chr17: 4,784,345-4,921,037 CHRNE, PLD2, 7 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4632235copy number variation1nstd183human GRCh37 chr17: 4,719,714-4,720,573 , GRCh38.p12 chr17: 4,816,419-4,817,278 PLD2
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4457587copy number variation1nstd102humanUncertain significance GRCh37 chr17: 3,759,126-6,128,911 , GRCh38.p12 chr17: 3,855,832-6,225,591 DERL2, ZZEF1, 82 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
    nsv4333060sequence alteration1nstd166human GRCh37.p13 chr17: 4,716,799-4,718,188 , GRCh38.p12 chr17: 4,813,504-4,814,893 PLD2
    nsv4238987copy number variation1nstd166human GRCh37.p13 chr17: 4,719,458-4,720,983 , GRCh38.p12 chr17: 4,816,163-4,817,688 PLD2
    nsv3923881copy number variation1nstd102humanPathogenic NCBI36 chr17: 48,539-4,989,051 , GRCh37.p13 chr17: 48,539-5,048,327 , GRCh38.p12 chr17: 198,748-5,145,032 CAMKK1, MIR6776, 177 more genes
    nsv3923152copy number variation1nstd102humanPathogenic NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343 PSMB6, NUP88, 133 more genes
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