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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5943981copy number variation1nstd209human GRCh38 chr13: 40,808,646-40,808,818 , GRCh37.p13 chr13: 41,382,782-41,382,954 MIR621, TPTE2P5, 1 more genes
    nsv5726319mobile element insertion1nstd211human GRCh38 chr13: 40,803,902-40,803,902 , GRCh37.p13 chr13: 41,378,038-41,378,038 TPTE2P5, SLC25A15
    nsv5672803copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,367,353-41,367,427 , GRCh38.p12 chr13: 40,793,217-40,793,291 SLC25A15
    nsv5672568copy number variation1nstd102humanPathogenic GRCh37 chr13: 41,379,234-41,383,803 , GRCh38.p12 chr13: 40,805,098-40,809,667 SLC25A15, MIR621, 1 more genes
    nsv5649755insertion1nstd207human GRCh38 chr13: 40,808,646-40,808,646 , GRCh37.p13 chr13: 41,382,782-41,382,782 SLC25A15, TPTE2P5
    nsv5564510copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,053,605-115,108,528 , GRCh38.p12 chr13: 18,479,465-114,343,053 RN7SL272P, DIAPH3, 1333 more genes
    nsv5561763mobile element insertion1nstd206human GRCh38 chr13: 40,803,902-40,803,953 , GRCh37.p13 chr13: 41,378,038-41,378,089 TPTE2P5, SLC25A15
    nsv5512561copy number variation1nstd206human GRCh38 chr13: 40,790,496-40,790,602 , GRCh37.p13 chr13: 41,364,632-41,364,738 SLC25A15
    nsv5509764copy number variation1nstd206human GRCh38 chr13: 40,808,646-40,808,820 , GRCh37.p13 chr13: 41,382,782-41,382,956 TPTE2P5, SLC25A15, 1 more genes
    nsv5509603copy number variation1nstd206human GRCh38 chr13: 40,789,514-40,789,599 , GRCh37.p13 chr13: 41,363,650-41,363,735 SLC25A15
    nsv5508713copy number variation1nstd206human GRCh38 chr13: 40,804,000-40,832,106 , GRCh37.p13 chr13: 41,378,136-41,406,242 MIR621, TPTE2P5, 1 more genes
    nsv5502466copy number variation1nstd206human GRCh38 chr13: 40,800,473-40,800,537 , GRCh37.p13 chr13: 41,374,609-41,374,673 TPTE2P5, SLC25A15
    nsv5338500translocation1nstd200human GRCh37 chr13: 41,388,309-41,388,309 , GRCh37 chr13: 41,387,094-41,387,094 , GRCh38.p12 chr13: 40,814,173-40,814,173 , GRCh38.p12 chr13: 40,812,958-40,812,958 TPTE2P5, SLC25A15
    nsv5312835copy number variation1nstd204human GRCh38.p13 chr13: 40,808,620-40,808,845 , GRCh37.p13 chr13: 41,382,756-41,382,981 MIR621, SLC25A15, 1 more genes
    nsv5004513copy number variation1nstd200human GRCh38 chr13: 40,808,646-40,808,820 , GRCh37.p13 chr13: 41,382,782-41,382,956 SLC25A15, TPTE2P5, 1 more genes
    nsv5004512copy number variation1nstd200human GRCh38 chr13: 40,781,916-40,795,110 , GRCh37.p13 chr13: 41,356,052-41,369,246 SLC25A15, TPTE2P5
    nsv4997135copy number variation1nstd200human GRCh38 chr13: 40,808,865-40,808,991 , GRCh37.p13 chr13: 41,383,001-41,383,127 MIR621, SLC25A15, 1 more genes
    nsv4841766copy number variation1nstd200human GRCh37 chr13: 41,370,586-41,434,133 , GRCh38.p12 chr13: 40,796,450-40,859,997 MIR621, TPTE2P5, 1 more genes
    nsv4839171copy number variation1nstd200human GRCh37 chr13: 41,382,782-41,382,956 , GRCh38.p12 chr13: 40,808,646-40,808,820 MIR621, SLC25A15, 1 more genes
    nsv4838539copy number variation1nstd200human GRCh37 chr13: 41,383,001-41,383,127 , GRCh38.p12 chr13: 40,808,865-40,808,991 MIR621, SLC25A15, 1 more genes
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