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Items: 1 to 20 of 125

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5518045copy number variation1nstd206human GRCh38 chr19: 57,639,616-57,643,568 , GRCh37.p13 chr19: 58,150,984-58,154,936 ZNF211
    nsv5300321copy number variation1nstd204human GRCh38.p13 chr19: 57,611,939-57,641,301 , GRCh37.p13 chr19: 58,123,307-58,152,669 ZNF530, ZNF134, 1 more genes
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv5280624copy number variation1nstd204human GRCh38.p13 chr19: 57,527,801-57,913,300 , GRCh37.p13 chr19: 58,039,169-58,424,668 ZNF549, ZNF417, 19 more genes
    nsv5028201copy number variation1nstd200human GRCh38 chr19: 57,633,690-57,633,819 , GRCh37.p13 chr19: 58,145,058-58,145,187 ZNF211
    nsv5025012copy number variation1nstd200human GRCh38 chr19: 57,620,355-57,646,339 , GRCh37.p13 chr19: 58,131,723-58,157,707 ZNF134, ZNF211
    nsv4865380copy number variation1nstd200human GRCh37 chr19: 58,131,723-58,157,707 , GRCh38.p12 chr19: 57,620,355-57,646,339 ZNF211, ZNF134
    nsv4861506copy number variation1nstd200human GRCh37 chr19: 58,145,058-58,145,187 , GRCh38.p12 chr19: 57,633,690-57,633,819 ZNF211
    nsv4628868copy number variation1nstd183human GRCh37 chr19: 58,133,937-58,154,955 , GRCh38.p12 chr19: 57,622,569-57,643,587 ZNF134, ZNF211
    nsv4457732copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,952,073-58,661,581 , GRCh38.p12 chr19: 57,440,705-58,150,214 ZNF418, ZNF606-AS1, 39 more genes
    nsv4457626copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,092,045-58,686,148 , GRCh38.p12 chr19: 57,580,677-58,174,781 ZNF417, ZSCAN1, 30 more genes
    nsv4457535copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,054,819-58,410,552 , GRCh38.p12 chr19: 57,543,451-57,899,184 ZNF587B, ZNF530, 17 more genes
    nsv4417207copy number variation1nstd174human GRCh37 chr19: 58,129,458-58,158,890 , GRCh38.p12 chr19: 57,618,090-57,647,522 ZNF134, ZNF211
    nsv4367703copy number variation1nstd173human GRCh37 chr19: 58,129,644-58,154,305 , GRCh38.p12 chr19: 57,618,276-57,642,937 ZNF134, ZNF211
    nsv4264516copy number variation1nstd166human GRCh37.p13 chr19: 58,012,736-58,148,044 , GRCh38.p12 chr19: 57,501,368-57,636,676 ZNF134, ZNF211, 6 more genes
    nsv4260430copy number variation1nstd166human GRCh37.p13 chr19: 58,131,723-58,157,705 , GRCh38.p12 chr19: 57,620,355-57,646,337 ZNF134, ZNF211
    nsv3924817copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,057,811-58,401,314 , NCBI36 chr19: 62,749,623-63,093,126 , GRCh38 chr19: 57,546,443-57,889,946 ZNF211, FKBP1AP1, 17 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 RPL39P37, CCDC106, 556 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 OSCAR, FKBP1AP1, 535 more genes
    nsv3923613copy number variation1nstd102humanPathogenic GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382 ZNF71-SMIM17, MIR518E, 393 more genes
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