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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903712copy number variation1nstd209human GRCh38 chr3: 182,949,313-182,949,670 , GRCh37.p13 chr3: 182,667,101-182,667,458 DCUN1D1
    nsv5726578mobile element insertion1nstd211human GRCh38 chr3: 182,973,891-182,973,891 , GRCh37.p13 chr3: 182,691,679-182,691,679 DCUN1D1
    nsv5721451mobile element insertion1nstd211human GRCh38 chr3: 182,973,906-182,973,906 , GRCh37.p13 chr3: 182,691,694-182,691,694 DCUN1D1
    nsv5559228mobile element insertion1nstd206human GRCh38 chr3: 182,973,906-182,973,942 , GRCh37.p13 chr3: 182,691,694-182,691,730 DCUN1D1
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5343909translocation1nstd200human GRCh37 chr6: 158,638,648-158,638,648 , GRCh37 chr3: 182,655,047-182,655,047 , GRCh38.p12 chr6: 158,217,616-158,217,616 , GRCh38.p12 chr3: 182,937,259-182,937,259 DCUN1D1
    nsv5323326translocation1nstd204human GRCh38.p13 chr6: 158,217,616-158,217,616 , GRCh38.p13 chr3: 182,937,259-182,937,259 , GRCh37.p13 chr3: 182,655,047-182,655,047 , GRCh37.p13 chr6: 158,638,648-158,638,648 DCUN1D1
    nsv5196308mobile element insertion1nstd203human GRCh38 chr3: 182,937,268-182,937,268 , GRCh37.p13 chr3: 182,655,056-182,655,056 DCUN1D1
    nsv5189875mobile element insertion1nstd203human GRCh38 chr3: 182,973,896-182,973,906 , GRCh37.p13 chr3: 182,691,684-182,691,694 DCUN1D1
    nsv5081788mobile element insertion1nstd203human GRCh38 chr3: 182,951,006-182,951,033 , GRCh37.p13 chr3: 182,668,794-182,668,821 DCUN1D1
    nsv4924931copy number variation1nstd200human GRCh38 chr3: 182,924,912-182,937,731 , GRCh37.p13 chr3: 182,642,700-182,655,519 DCUN1D1
    nsv4921142copy number variation1nstd200human GRCh38 chr3: 182,983,656-182,985,527 , GRCh37.p13 chr3: 182,701,444-182,703,315 DCUN1D1, LOC105374246
    nsv4921141copy number variation1nstd200human GRCh38 chr3: 182,972,281-182,973,029 , GRCh37.p13 chr3: 182,690,069-182,690,817 DCUN1D1
    nsv4921140copy number variation1nstd200human GRCh38 chr3: 182,944,797-182,955,274 , GRCh37.p13 chr3: 182,662,585-182,673,062 DCUN1D1, C9orf85P2
    nsv4798861copy number variation1nstd200human GRCh37 chr3: 182,701,459-182,703,303 , GRCh38.p12 chr3: 182,983,671-182,985,515 LOC105374246, DCUN1D1
    nsv4798860copy number variation1nstd200human GRCh37 chr3: 182,662,585-182,673,062 , GRCh38.p12 chr3: 182,944,797-182,955,274 C9orf85P2, DCUN1D1
    nsv4769308copy number variation1nstd102humanPathogenic GRCh37 chr3: 180,834,336-183,551,661 , GRCh38.p12 chr3: 181,116,548-183,833,873 SNORD3P4, B3GNT5, 43 more genes
    nsv4769252copy number variation1nstd102humanPathogenic GRCh37 chr3: 181,171,210-184,706,091 , GRCh38.p12 chr3: 181,453,422-184,988,303 LOC107986054, LOC107986160, 83 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4588063copy number variation1nstd183human GRCh37 chr3: 182,698,349-182,698,673 , GRCh38.p12 chr3: 182,980,561-182,980,885 LOC105374246, DCUN1D1
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