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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5177927mobile element insertion1nstd203human GRCh38 chr19: 1,448,384-1,448,402 , GRCh37.p13 chr19: 1,448,383-1,448,401 APC2
    nsv5019054copy number variation1nstd200human GRCh38 chr19: 1,440,873-1,444,938 , GRCh37.p13 chr19: 1,440,872-1,444,937 RPS15, APC2
    nsv4868110copy number variation1nstd200human GRCh37 chr19: 1,440,872-1,444,937 , GRCh38.p12 chr19: 1,440,873-1,444,938 APC2, RPS15
    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
    nsv4623769copy number variation2nstd183human GRCh37 chr19: 1,465,058-1,470,715 , GRCh38.p12 chr19: 1,465,059-1,470,716 APC2
    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
    nsv4499093mobile element insertion1nstd166human GRCh37.p13 chr19: 1,447,570-1,447,570 , GRCh38.p12 chr19: 1,447,571-1,447,571 APC2
    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
    nsv4420249copy number variation1nstd174human GRCh37 chr19: 1,465,058-1,472,330 , GRCh38.p12 chr19: 1,465,059-1,472,331 C19orf25, APC2
    nsv4267210copy number variation1nstd166human GRCh37.p13 chr19: 1,440,872-1,444,937 , GRCh38.p12 chr19: 1,440,873-1,444,938 APC2, RPS15
    nsv4259462copy number variation1nstd166human GRCh37.p13 chr19: 1,446,293-1,446,439 , GRCh38.p12 chr19: 1,446,294-1,446,440 APC2
    nsv3955463insertion1nstd168human GRCh38 chr19: 1,449,533-1,554,193 , GRCh37.p13 chr19: 1,449,532-1,554,192 APC2, PCSK4, 6 more genes
    nsv3938966insertion1nstd167human GRCh37 chr19: 1,455,933-1,455,933 , GRCh38.p12 chr19: 1,455,934-1,455,934 APC2
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