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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137767copy number variation1nstd102humanPathogenic GRCh37 chr10: 126,093,215-126,094,107 , GRCh38 chr10: 124,404,646-124,405,538 OAT
    nsv6112765copy number variation1nstd102humanPathogenic GRCh37 chr10: 118,247,181-135,435,319 , GRCh38.p12 chr10: 116,487,669-133,621,815 STK32C, LOC105378542, 266 more genes
    nsv5980446copy number variation1nstd102humanPathogenic GRCh37 chr10: 122,785,023-135,457,222 , GRCh38.p12 chr10: 121,025,510-133,643,718 LINC02641, CFAP46, 194 more genes
    nsv5708166mobile element insertion1nstd211human GRCh38 chr10: 124,401,023-124,401,023 , GRCh37.p13 chr10: 126,089,592-126,089,592 OAT
    nsv5701368mobile element insertion1nstd211human GRCh38 chr10: 124,406,145-124,406,145 , GRCh37.p13 chr10: 126,094,714-126,094,714 OAT
    nsv5695110mobile element insertion2nstd211human GRCh38 chr10: 124,415,289-124,415,289 , GRCh37.p13 chr10: 126,103,858-126,103,858 OAT
    nsv5672686copy number variation1nstd102humanPathogenic GRCh37 chr10: 126,093,995-126,100,239 , GRCh38.p12 chr10: 124,405,426-124,411,670 OAT
    nsv5411601mobile element insertion1nstd206human GRCh38 chr10: 124,415,289-124,415,340 , GRCh37.p13 chr10: 126,103,858-126,103,909 OAT
    nsv5406361mobile element insertion1nstd206human GRCh38 chr10: 124,406,145-124,406,196 , GRCh37.p13 chr10: 126,094,714-126,094,765 OAT
    nsv5135752mobile element insertion1nstd203human GRCh38 chr10: 124,415,289-124,415,289 , GRCh37.p13 chr10: 126,103,858-126,103,858 OAT
    nsv5127849mobile element insertion1nstd203human GRCh38 chr10: 124,406,128-124,406,145 , GRCh37.p13 chr10: 126,094,697-126,094,714 OAT
    nsv4983961copy number variation1nstd200human GRCh38 chr10: 124,413,460-124,414,652 , GRCh37.p13 chr10: 126,102,029-126,103,221 OAT
    nsv4836830copy number variation1nstd200human GRCh37 chr10: 126,102,029-126,103,221 , GRCh38.p12 chr10: 124,413,460-124,414,652 OAT
    nsv4675991copy number variation1nstd102humanPathogenic GRCh37 chr10: 119,996,339-135,427,143 , GRCh38.p12 chr10: 118,236,827-133,613,639 STK32C, LOC105378542, 237 more genes
    nsv4666799copy number variation1nstd186human GRCh37 chr10: 126,097,074-126,100,798 , GRCh38.p12 chr10: 124,408,505-124,412,229 OAT
    nsv4666765copy number variation1nstd186human GRCh37 chr10: 126,097,616-126,100,798 , GRCh38.p12 chr10: 124,409,047-124,412,229 OAT
    nsv4613211copy number variation1nstd183human GRCh37 chr10: 126,097,236-126,107,533 , GRCh38.p12 chr10: 124,408,667-124,418,964 OAT
    nsv4609320copy number variation1nstd183human GRCh37 chr10: 126,086,273-126,089,602 , GRCh38.p12 chr10: 124,397,704-124,401,033 OAT
    nsv4602552copy number variation1nstd183human GRCh37 chr10: 126,097,074-126,100,798 , GRCh38.p12 chr10: 124,408,505-124,412,229 OAT
    nsv4601572copy number variation1nstd183human GRCh37 chr10: 126,097,616-126,100,798 , GRCh38.p12 chr10: 124,409,047-124,412,229 OAT
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