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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5713899mobile element insertion2nstd211human GRCh38 chr17: 5,400,157-5,400,157 , GRCh37.p13 chr17: 5,303,477-5,303,477 NUP88
    nsv5527572copy number variation1nstd206human GRCh38 chr17: 5,384,678-5,384,739 , GRCh37.p13 chr17: 5,287,998-5,288,059 RABEP1, NUP88
    nsv5145911mobile element insertion1nstd203human GRCh38 chr17: 5,394,735-5,394,751 , GRCh37.p13 chr17: 5,298,055-5,298,071 NUP88
    nsv5023590copy number variation1nstd200human GRCh38 chr17: 5,094,869-5,399,676 , GRCh37.p13 chr17: 4,998,164-5,302,996 LOC105371505, ZNF232-AS1, 8 more genes
    nsv5015642copy number variation1nstd200human GRCh38 chr17: 5,409,137-5,410,458 , GRCh37.p13 chr17: 5,312,457-5,313,778 NUP88
    nsv5015641copy number variation1nstd200human GRCh38 chr17: 5,407,104-5,407,163 , GRCh37.p13 chr17: 5,310,424-5,310,483 NUP88
    nsv5015640copy number variation1nstd200human GRCh38 chr17: 5,400,455-5,403,372 , GRCh37.p13 chr17: 5,303,775-5,306,692 NUP88
    nsv4857857copy number variation1nstd200human GRCh37 chr17: 5,303,775-5,306,692 , GRCh38.p12 chr17: 5,400,455-5,403,372 NUP88
    nsv4857856copy number variation1nstd200human GRCh37 chr17: 5,296,704-5,297,019 , GRCh38.p12 chr17: 5,393,384-5,393,699 NUP88
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729877copy number variation1nstd102humanUncertain significance GRCh37 chr17: 5,143,295-5,850,209 , GRCh38.p12 chr17: 5,240,000-5,946,889 DHX33, MIS12, 14 more genes
    nsv4707695copy number variation1nstd195human GRCh37 chr17: 5,303,772-5,303,773 , GRCh38.p12 chr17: 5,400,452-5,400,453 NUP88
    nsv4706001copy number variation1nstd195human GRCh37 chr17: 5,303,477-5,303,478 , GRCh38.p12 chr17: 5,400,157-5,400,158 NUP88
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4630208copy number variation1nstd183human GRCh37 chr17: 4,486,568-5,620,052 , GRCh38.p12 chr17: 4,583,273-5,716,732 , ARRB2, 59 more genes
    nsv4627871copy number variation1nstd183human GRCh37 chr17: 5,287,053-5,288,214 , GRCh38.p12 chr17: 5,383,733-5,384,894 RABEP1, NUP88
    nsv4555322insertion1nstd166human GRCh37.p13 chr17: 5,322,040-5,322,040 , GRCh38.p12 chr17: 5,418,720-5,418,720 RPAIN, NUP88
    nsv4512107mobile element insertion1nstd166human GRCh37.p13 chr17: 5,294,460-5,294,460 , GRCh38.p12 chr17: 5,391,140-5,391,140 NUP88
    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
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