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Items: 1 to 20 of 260

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978296inversion1nstd209human GRCh38 chr17: 81,945,255-82,544,213 , GRCh37.p13 chr17: 79,903,131-80,502,089 , CD7, 29 more genes
    nsv5943958copy number variation1nstd209human GRCh38 chr17: 82,260,288-82,260,350 , GRCh37.p13 chr17: 80,218,164-80,218,226 CSNK1D
    nsv5931652copy number variation1nstd209human GRCh38 chr17: 82,259,954-82,260,016 , GRCh37.p13 chr17: 80,217,830-80,217,892 CSNK1D
    nsv5662970insertion1nstd207human GRCh38 chr17: 82,254,989-82,254,989 , GRCh37.p13 chr17: 80,212,865-80,212,865 CSNK1D
    nsv5661562insertion1nstd207human GRCh38 chr17: 82,260,017-82,260,017 , GRCh37.p13 chr17: 80,217,893-80,217,893 CSNK1D
    nsv5659829insertion1nstd207human GRCh38 chr17: 82,260,658-82,260,658 , GRCh37.p13 chr17: 80,218,534-80,218,534 CSNK1D
    nsv5602801copy number variation1nstd207human GRCh38 chr17: 82,254,433-82,254,656 , GRCh37.p13 chr17: 80,212,309-80,212,532 CSNK1D
    nsv5600589copy number variation1nstd207human GRCh38 chr17: 82,260,288-82,260,350 , GRCh37.p13 chr17: 80,218,164-80,218,226 CSNK1D
    nsv5556495sequence alteration1nstd206human GRCh38 chr17: 81,945,298-82,544,214 , GRCh37.p13 chr17: 79,903,174-80,502,090 , RAC3, 29 more genes
    nsv5533590copy number variation1nstd206human GRCh38 chr17: 82,260,366-82,260,849 , GRCh37.p13 chr17: 80,218,242-80,218,725 CSNK1D
    nsv5524295copy number variation1nstd206human GRCh38 chr17: 82,274,146-82,274,257 , GRCh37.p13 chr17: 80,232,022-80,232,133 CSNK1D
    nsv5516322copy number variation1nstd206human GRCh38 chr17: 82,248,092-82,248,190 , GRCh37.p13 chr17: 80,205,968-80,206,066 CSNK1D
    nsv5325693copy number variation1nstd204human GRCh38.p13 chr17: 82,254,518-82,255,229 , GRCh37.p13 chr17: 80,212,394-80,213,105 CSNK1D
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5297201copy number variation1nstd204human GRCh38.p13 chr17: 82,242,541-82,284,874 , GRCh37.p13 chr17: 80,200,417-80,242,750 CSNK1D
    nsv5294422copy number variation1nstd204human GRCh37.p13 chr17: 80,112,777-80,311,976 , GRCh38.p13 chr17: 82,154,901-82,354,100 , CD7, 6 more genes
    nsv5281724copy number variation1nstd204human GRCh38.p13 chr17: 82,258,201-82,290,300 , GRCh37.p13 chr17: 80,216,077-80,248,176 LINC01970, CSNK1D
    nsv5017096copy number variation1nstd200human GRCh38 chr17: 82,253,753-82,254,846 , GRCh37.p13 chr17: 80,211,629-80,212,722 CSNK1D
    nsv5017095copy number variation1nstd200human GRCh38 chr17: 82,234,285-82,238,173 , GRCh37.p13 chr17: 80,192,161-80,196,049 SLC16A3, MIR6787, 1 more genes
    nsv5014130copy number variation1nstd200human GRCh38 chr17: 82,159,811-82,579,676 , GRCh37.p13 chr17: 80,117,687-80,537,552 , LINC01970, 17 more genes
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