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Items: 1 to 20 of 338

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5972752inversion1nstd209human GRCh38 chr13: 97,456,271-97,456,712 , GRCh37.p13 chr13: 98,108,525-98,108,966 RAP2A
    nsv5940414copy number variation1nstd209human GRCh38 chr13: 97,434,783-97,464,202 , GRCh37.p13 chr13: 98,087,037-98,116,456 RAP2A
    nsv5931376copy number variation1nstd209human GRCh38 chr13: 97,451,637-97,456,153 , GRCh37.p13 chr13: 98,103,891-98,108,407 RAP2A
    nsv5855404copy number variation1nstd209human GRCh38 chr13: 97,451,624-97,456,106 , GRCh37.p13 chr13: 98,103,878-98,108,360 RAP2A
    nsv5850375copy number variation1nstd209human GRCh38 chr13: 97,464,472-97,466,697 , GRCh37.p13 chr13: 98,116,726-98,118,951 RAP2A
    nsv5847570copy number variation1nstd209human GRCh38 chr13: 97,468,953-97,471,366 , GRCh37.p13 chr13: 98,121,207-98,123,620 RAP2A
    nsv5672807copy number variation1nstd102humanPathogenic GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964 RPL7L1P12, MIR548AS, 153 more genes
    nsv5672796copy number variation1nstd102humanPathogenic GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798 LINC00359, LOC107984609, 220 more genes
    nsv5671538inversion1nstd207human GRCh38 chr13: 97,456,278-97,456,715 , GRCh37.p13 chr13: 98,108,532-98,108,969 RAP2A
    nsv5658361insertion1nstd207human GRCh38 chr13: 97,456,698-97,456,698 , GRCh37.p13 chr13: 98,108,952-98,108,952 RAP2A
    nsv5598135copy number variation1nstd207human GRCh38 chr13: 97,456,296-97,456,589 , GRCh37.p13 chr13: 98,108,550-98,108,843 RAP2A
    nsv5587999copy number variation1nstd207human GRCh38 chr13: 97,451,637-97,456,153 , GRCh37.p13 chr13: 98,103,891-98,108,407 RAP2A
    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
    nsv5562456inversion1nstd206human GRCh38 chr13: 97,456,255-97,456,733 , GRCh37.p13 chr13: 98,108,509-98,108,987 RAP2A
    nsv5561291sequence alteration1nstd206human GRCh38 chr13: 97,451,702-97,456,783 , GRCh37.p13 chr13: 98,103,956-98,109,037 RAP2A
    nsv5553180insertion1nstd206human GRCh38 chr13: 97,461,949-97,461,972 , GRCh37.p13 chr13: 98,114,203-98,114,226 RAP2A
    nsv5506022copy number variation1nstd206human GRCh38 chr13: 97,451,622-97,456,174 , GRCh37.p13 chr13: 98,103,876-98,108,428 RAP2A
    nsv5391408copy number variation3nstd186human GRCh37 chr13: 98,103,896-98,108,408 , GRCh38.p12 chr13: 97,451,642-97,456,154 RAP2A
    nsv5374359translocation1nstd200human GRCh38 chr13: 97,469,432-97,469,432 , GRCh38 chr13: 97,473,589-97,473,589 , GRCh37.p13 chr13: 98,121,686-98,121,686 , GRCh37.p13 chr13: 98,125,843-98,125,843 RAP2A
    nsv5321258inversion1nstd204human GRCh38.p13 chr13: 97,456,276-97,456,714 , GRCh37.p13 chr13: 98,108,530-98,108,968 RAP2A
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