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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959078insertion1nstd209human GRCh38 chr9: 111,769,985-111,769,985 , GRCh37.p13 chr9: 114,532,265-114,532,265 SHOC1
    nsv5924410copy number variation1nstd209human GRCh38 chr9: 111,494,845-111,906,694 , GRCh37.p13 chr9: 114,257,125-114,668,974 UGCG, PTGR1, 8 more genes
    nsv5921625copy number variation1nstd209human GRCh38 chr9: 111,791,752-111,791,867 , GRCh37.p13 chr9: 114,554,032-114,554,147 SHOC1
    nsv5727767mobile element insertion2nstd211human GRCh38 chr9: 111,700,752-111,700,752 , GRCh37.p13 chr9: 114,463,032-114,463,032 SHOC1
    nsv5725447mobile element insertion1nstd211human GRCh38 chr9: 111,706,214-111,706,214 , GRCh37.p13 chr9: 114,468,494-114,468,494 SHOC1
    nsv5723410mobile element insertion1nstd211human GRCh38 chr9: 111,760,636-111,760,636 , GRCh37.p13 chr9: 114,522,916-114,522,916 SHOC1
    nsv5710697mobile element insertion1nstd211human GRCh38 chr9: 111,701,170-111,701,170 , GRCh37.p13 chr9: 114,463,450-114,463,450 SHOC1
    nsv5709807mobile element insertion1nstd211human GRCh38 chr9: 111,781,753-111,781,753 , GRCh37.p13 chr9: 114,544,033-114,544,033 SHOC1
    nsv5695357mobile element insertion1nstd211human GRCh38 chr9: 111,751,548-111,751,548 , GRCh37.p13 chr9: 114,513,828-114,513,828 SHOC1
    nsv5694545mobile element insertion1nstd211human GRCh38 chr9: 111,781,831-111,781,831 , GRCh37.p13 chr9: 114,544,111-114,544,111 SHOC1
    nsv5642343insertion1nstd207human GRCh38 chr9: 111,781,831-111,781,831 , GRCh37.p13 chr9: 114,544,111-114,544,111 SHOC1
    nsv5602679copy number variation1nstd207human GRCh38 chr9: 111,791,752-111,791,809 , GRCh37.p13 chr9: 114,554,032-114,554,089 SHOC1
    nsv5562556mobile element insertion1nstd206human GRCh38 chr9: 111,700,752-111,700,803 , GRCh37.p13 chr9: 114,463,032-114,463,083 SHOC1
    nsv5560542mobile element insertion1nstd206human GRCh38 chr9: 111,706,214-111,706,265 , GRCh37.p13 chr9: 114,468,494-114,468,545 SHOC1
    nsv5402855mobile element insertion1nstd206human GRCh38 chr9: 111,751,548-111,751,592 , GRCh37.p13 chr9: 114,513,828-114,513,872 SHOC1
    nsv5400401mobile element insertion1nstd206human GRCh38 chr9: 111,701,170-111,701,221 , GRCh37.p13 chr9: 114,463,450-114,463,501 SHOC1
    nsv5396659mobile element insertion1nstd206human GRCh38 chr9: 111,781,847-111,781,882 , GRCh37.p13 chr9: 114,544,127-114,544,162 SHOC1
    nsv5372983translocation1nstd200human GRCh38 chr9: 111,754,092-111,754,092 , GRCh38 chr9: 111,754,033-111,754,033 , GRCh37.p13 chr9: 114,516,313-114,516,313 , GRCh37.p13 chr9: 114,516,372-114,516,372 SHOC1
    nsv5197663mobile element insertion1nstd203human GRCh38 chr9: 111,700,736-111,700,752 , GRCh37.p13 chr9: 114,463,016-114,463,032 SHOC1
    nsv5188453mobile element insertion1nstd203human GRCh38 chr9: 111,765,159-111,765,172 , GRCh37.p13 chr9: 114,527,439-114,527,452 SHOC1
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