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Items: 1 to 20 of 618

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6121798copy number variation1nstd186human GRCh37 chr14: 71,450,310-71,451,351 , GRCh38.p12 chr14: 70,983,593-70,984,634 PCNX1
    nsv6117163mobile element insertion1nstd186human GRCh37 chr14: 71,446,221-71,446,272 , GRCh38.p12 chr14: 70,979,504-70,979,555 PCNX1
    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
    nsv5976794insertion1nstd209human GRCh38 chr14: 70,949,269-70,949,269 , GRCh37.p13 chr14: 71,415,986-71,415,986 PCNX1, LOC105370557
    nsv5974376insertion1nstd209human GRCh38 chr14: 71,013,550-71,013,550 , GRCh37.p13 chr14: 71,480,267-71,480,267 PCNX1
    nsv5972841insertion1nstd209human GRCh38 chr14: 71,003,080-71,003,080 , GRCh37.p13 chr14: 71,469,797-71,469,797 PCNX1
    nsv5945026copy number variation1nstd209human GRCh38 chr14: 71,068,635-71,068,838 , GRCh37.p13 chr14: 71,535,352-71,535,555 PCNX1
    nsv5939808copy number variation1nstd209human GRCh38 chr14: 70,971,110-70,971,442 , GRCh37.p13 chr14: 71,437,827-71,438,159 PCNX1
    nsv5931784copy number variation1nstd209human GRCh38 chr14: 70,983,551-70,984,633 , GRCh37.p13 chr14: 71,450,268-71,451,350 PCNX1
    nsv5855828copy number variation1nstd209human GRCh38 chr14: 70,983,560-70,984,689 , GRCh37.p13 chr14: 71,450,277-71,451,406 PCNX1
    nsv5712983mobile element insertion2nstd211human GRCh38 chr14: 70,979,504-70,979,504 , GRCh37.p13 chr14: 71,446,221-71,446,221 PCNX1
    nsv5710689mobile element insertion2nstd211human GRCh38 chr14: 70,962,019-70,962,019 , GRCh37.p13 chr14: 71,428,736-71,428,736 PCNX1, LOC105370557
    nsv5710516mobile element insertion1nstd211human GRCh38 chr14: 71,076,034-71,076,034 , GRCh37.p13 chr14: 71,542,751-71,542,751 PCNX1
    nsv5708604mobile element insertion1nstd211human GRCh38 chr14: 70,910,716-70,910,716 , GRCh37.p13 chr14: 71,377,433-71,377,433 PCNX1
    nsv5706079mobile element insertion2nstd211human GRCh38 chr14: 71,013,567-71,013,567 , GRCh37.p13 chr14: 71,480,284-71,480,284 PCNX1
    nsv5662845insertion1nstd207human GRCh38 chr14: 71,021,052-71,021,052 , GRCh37.p13 chr14: 71,487,769-71,487,769 PCNX1
    nsv5662511insertion1nstd207human GRCh38 chr14: 70,910,097-70,910,097 , GRCh37.p13 chr14: 71,376,814-71,376,814 PCNX1
    nsv5656303insertion1nstd207human GRCh38 chr14: 71,013,550-71,013,550 , GRCh37.p13 chr14: 71,480,267-71,480,267 PCNX1
    nsv5649396insertion1nstd207human GRCh38 chr14: 70,949,111-70,949,111 , GRCh37.p13 chr14: 71,415,828-71,415,828 PCNX1, LOC105370557
    nsv5600956copy number variation1nstd207human GRCh38 chr14: 71,068,635-71,068,838 , GRCh37.p13 chr14: 71,535,352-71,535,555 PCNX1
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