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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980451copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321 ACTN1, ACYP1, 400 more genes
    nsv5509643copy number variation1nstd206human GRCh38 chr14: 70,654,360-70,655,231 , GRCh37.p13 chr14: 71,121,077-71,121,948 TTC9
    nsv5506017copy number variation1nstd206human GRCh38 chr14: 70,642,075-70,642,126 , GRCh37.p13 chr14: 71,108,792-71,108,843 TTC9
    nsv5496517copy number variation1nstd206human GRCh38 chr14: 70,655,252-70,657,761 , GRCh37.p13 chr14: 71,121,969-71,124,478 TTC9
    nsv5374597translocation1nstd200human GRCh38 chr14: 70,657,768-70,657,768 , GRCh38 chr14: 70,655,253-70,655,253 , GRCh37.p13 chr14: 71,124,485-71,124,485 , GRCh37.p13 chr14: 71,121,970-71,121,970 TTC9
    nsv5305740copy number variation1nstd204human GRCh38.p13 chr14: 70,654,049-70,655,568 , GRCh37.p13 chr14: 71,120,766-71,122,285 TTC9
    nsv5159723mobile element insertion1nstd203human GRCh38 chr14: 70,654,594-70,654,622 , GRCh37.p13 chr14: 71,121,311-71,121,339 TTC9
    nsv5147623mobile element insertion1nstd203human GRCh38 chr14: 70,657,259-70,657,267 , GRCh37.p13 chr14: 71,123,976-71,123,984 TTC9
    nsv5145445mobile element insertion1nstd203human GRCh38 chr14: 70,654,601-70,654,622 , GRCh37.p13 chr14: 71,121,318-71,121,339 TTC9
    nsv5140779mobile element insertion1nstd203human GRCh38 chr14: 70,654,587-70,654,622 , GRCh37.p13 chr14: 71,121,304-71,121,339 TTC9
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004748copy number variation1nstd200human GRCh38 chr14: 70,675,354-70,999,301 , GRCh37.p13 chr14: 71,142,071-71,466,018 LINC01269, MAP3K9, 5 more genes
    nsv5004747copy number variation1nstd200human GRCh38 chr14: 70,653,267-70,653,429 , GRCh37.p13 chr14: 71,119,984-71,120,146 TTC9
    nsv4999913copy number variation1nstd200human GRCh38 chr14: 70,655,204-70,655,373 , GRCh37.p13 chr14: 71,121,921-71,122,090 TTC9
    nsv4844678copy number variation1nstd200human GRCh37 chr14: 71,121,966-71,124,519 , GRCh38.p12 chr14: 70,655,249-70,657,802 TTC9
    nsv4842448copy number variation1nstd200human GRCh37 chr14: 71,121,067-71,121,989 , GRCh38.p12 chr14: 70,654,350-70,655,272 TTC9
    nsv4626297copy number variation1nstd183human GRCh37 chr14: 71,121,917-71,124,485 , GRCh38.p12 chr14: 70,655,200-70,657,768 TTC9
    nsv4562614mobile element insertion1nstd166human GRCh37.p13 chr14: 71,118,255-71,118,255 , GRCh38.p12 chr14: 70,651,538-70,651,538 TTC9
    nsv4513524mobile element insertion1nstd166human GRCh37.p13 chr14: 71,108,159-71,108,159 , GRCh38.p12 chr14: 70,641,442-70,641,442 TTC9, TTC9-DT
    nsv4414318copy number variation1nstd174human GRCh37 chr14: 71,121,895-71,124,582 , GRCh38.p12 chr14: 70,655,178-70,657,865 TTC9
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