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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944551copy number variation1nstd209human GRCh38 chr19: 1,480,837-1,481,037 , GRCh37.p13 chr19: 1,480,836-1,481,036 PCSK4
    nsv5673303copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,486,852-1,491,383 , GRCh38.p12 chr19: 1,486,853-1,491,384 PCSK4, REEP6
    nsv5323128copy number variation1nstd204human GRCh38.p13 chr19: 1,480,837-1,481,057 , GRCh37.p13 chr19: 1,480,836-1,481,056 PCSK4
    nsv5291342copy number variation1nstd204human GRCh38.p13 chr19: 879,901-2,550,600 , GRCh37.p13 chr19: 879,901-2,550,598 LOC105372240, ELOCP28, 92 more genes
    nsv5284613copy number variation1nstd204human GRCh38.p13 chr19: 1,402,101-1,628,800 , GRCh37.p13 chr19: 1,402,100-1,628,799 TCF3, RN7SL477P, 13 more genes
    nsv5283415copy number variation1nstd204human GRCh37.p13 chr19: 1,478,200-1,534,699 , GRCh38.p13 chr19: 1,478,201-1,534,700 PCSK4, REEP6, 4 more genes
    nsv5019055copy number variation1nstd200human GRCh38 chr19: 1,483,054-1,485,841 , GRCh37.p13 chr19: 1,483,053-1,485,840 PCSK4
    nsv4727908copy number variation1nstd197human GRCh38.p12 chr19: 1,461,038-1,483,941 , GRCh37 chr19: 1,461,037-1,483,940 APC2, PCSK4, 1 more genes
    nsv4676366copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 1,075,192-2,256,387 , GRCh38.p12 chr19: 1,075,193-2,256,388 AMH, ATP5F1D, 64 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 AZU1, REEP6, 159 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4667696copy number variation1nstd186human GRCh37 chr19: 1,483,842-1,484,049 , GRCh38.p12 chr19: 1,483,843-1,484,050 PCSK4
    nsv4634254copy number variation1nstd183human GRCh37 chr19: 1,483,842-1,484,049 , GRCh38.p12 chr19: 1,483,843-1,484,050 PCSK4
    nsv4633640copy number variation1nstd183human GRCh37 chr19: 1,483,901-1,487,026 , GRCh38.p12 chr19: 1,483,902-1,487,027 PCSK4
    nsv4623195copy number variation1nstd183human GRCh37 chr19: 1,468,438-1,512,978 , GRCh38.p12 chr19: 1,468,439-1,512,979 ADAMTSL5, APC2, 3 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
    nsv4457632copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,342,624-1,817,866 , GRCh38.p12 chr19: 1,342,625-1,817,867 ONECUT3, UQCR11, 23 more genes
    nsv4452268copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,406,030-3,597,207 , GRCh38.p12 chr19: 1,406,031-3,597,209 C19orf25, MIR7108, 92 more genes
    nsv4415618copy number variation1nstd174human GRCh37 chr19: 1,486,558-1,516,997 , GRCh38.p12 chr19: 1,486,559-1,516,998 REEP6, LOC107985337, 2 more genes
    nsv4265634copy number variation1nstd166human GRCh37.p13 chr19: 1,483,806-1,483,900 , GRCh38.p12 chr19: 1,483,807-1,483,901 PCSK4
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