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Items: 1 to 20 of 105

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5951271insertion1nstd209human GRCh38 chr5: 157,139,720-157,139,720 , GRCh37.p13 chr5: 156,566,731-156,566,731 MED7
    nsv5898260copy number variation1nstd209human GRCh38 chr5: 156,986,485-157,423,872 , GRCh37.p13 chr5: 156,413,496-156,850,880 ITK, MED7, 7 more genes
    nsv5678915mobile element insertion2nstd211human GRCh38 chr5: 157,139,729-157,139,729 , GRCh37.p13 chr5: 156,566,740-156,566,740 MED7
    nsv5627989insertion1nstd207human GRCh38 chr5: 157,139,720-157,139,720 , GRCh37.p13 chr5: 156,566,731-156,566,731 MED7
    nsv5537432insertion1nstd206human GRCh38 chr5: 157,139,720-157,139,720 , GRCh37.p13 chr5: 156,566,731-156,566,731 MED7
    nsv5463404copy number variation1nstd206human GRCh38 chr5: 157,143,022-157,144,675 , GRCh37.p13 chr5: 156,570,033-156,571,686 MED7
    nsv5099686mobile element insertion1nstd203human GRCh38 chr5: 157,139,719-157,139,729 , GRCh37.p13 chr5: 156,566,730-156,566,740 MED7
    nsv5097870mobile element insertion1nstd203human GRCh38 chr5: 157,139,724-157,139,729 , GRCh37.p13 chr5: 156,566,735-156,566,740 MED7
    nsv5086748mobile element insertion1nstd203human GRCh38 chr5: 157,139,716-157,139,729 , GRCh37.p13 chr5: 156,566,727-156,566,740 MED7
    nsv5085693mobile element insertion1nstd203human GRCh38 chr5: 157,139,723-157,139,729 , GRCh37.p13 chr5: 156,566,734-156,566,740 MED7
    nsv5085242mobile element insertion1nstd203human GRCh38 chr5: 157,139,725-157,139,729 , GRCh37.p13 chr5: 156,566,736-156,566,740 MED7
    nsv5082498mobile element insertion1nstd203human GRCh38 chr5: 157,139,720-157,139,729 , GRCh37.p13 chr5: 156,566,731-156,566,740 MED7
    nsv5080792mobile element insertion1nstd203human GRCh38 chr5: 157,139,727-157,139,729 , GRCh37.p13 chr5: 156,566,738-156,566,740 MED7
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4751125insertion1nstd199human GRCh37 chr5: 156,566,735-156,566,735 , GRCh38.p12 chr5: 157,139,724-157,139,724 MED7
    nsv4719530insertion1nstd186human GRCh37 chr5: 156,566,731-156,566,731 , GRCh38.p12 chr5: 157,139,720-157,139,720 MED7
    nsv4687219mobile element insertion1nstd186human GRCh37 chr5: 156,566,740-156,566,740 , GRCh38.p12 chr5: 157,139,729-157,139,729 MED7
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4549091insertion1nstd166human GRCh37.p13 chr5: 156,566,731-156,566,731 , GRCh38.p12 chr5: 157,139,720-157,139,720 MED7
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