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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094266copy number variation1nstd102humanUncertain significance GRCh37 chr14: 76,088,402-76,174,070 , GRCh38.p12 chr14: 75,622,059-75,707,727 TTLL5, FLVCR2, 1 more genes
    nsv6974940copy number variation1nstd229human GRCh38 chr14: 75,523,370-76,313,567 , GRCh37.p13 chr14: 75,989,713-76,779,910 LOC107984653, LOC100506576, 13 more genes
    nsv6964648copy number variation1nstd229human GRCh38 chr14: 75,255,601-75,729,300 , GRCh37.p13 chr14: 75,722,304-76,195,643 LOC107984653, ERG28, 12 more genes
    nsv6964550copy number variation1nstd229human GRCh38 chr14: 75,660,529-75,666,768 , GRCh37.p13 chr14: 76,126,872-76,133,111 ERG28, TTLL5
    nsv6960070copy number variation1nstd229human GRCh38 chr14: 75,639,481-75,881,240 , GRCh37.p13 chr14: 76,105,824-76,347,583 ERG28, RPS2P43, 2 more genes
    nsv6958124copy number variation1nstd229human GRCh38 chr14: 75,651,889-75,654,884 , GRCh37.p13 chr14: 76,118,232-76,121,227 ERG28
    nsv6581484inversion1nstd223human GRCh38 chr14: 75,652,938-75,653,516 , GRCh37.p13 chr14: 76,119,281-76,119,859 ERG28
    nsv6492140copy number variation1nstd223human GRCh38 chr14: 75,648,029-75,649,563 , GRCh37.p13 chr14: 76,114,372-76,115,906 FLVCR2, ERG28
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6309706copy number variation1nstd102humanUncertain significance GRCh37 chr14: 76,090,935-76,187,066 , GRCh38.p12 chr14: 75,624,592-75,720,723 TTLL5, FLVCR2, 1 more genes
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4627767copy number variation1nstd183human GRCh37 chr14: 76,023,819-76,300,735 , GRCh38.p12 chr14: 75,557,476-75,834,392 , ERG28, 6 more genes
    nsv4515437mobile element insertion1nstd166human GRCh37.p13 chr14: 76,126,695-76,126,695 , GRCh38.p12 chr14: 75,660,352-75,660,352 ERG28, TTLL5
    nsv4501073mobile element insertion1nstd166human GRCh37.p13 chr14: 76,120,941-76,120,941 , GRCh38.p12 chr14: 75,654,598-75,654,598 ERG28
    nsv4456104copy number variation1nstd102humanUncertain significance GRCh37 chr14: 76,057,971-76,576,494 , GRCh38.p12 chr14: 75,591,628-76,110,151 RPS24P2, TGFB3, 8 more genes
    nsv4349747copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 74,040,231-76,368,547 , GRCh38.p12 chr14: 73,573,527-75,902,204 ACYP1, ENTPD5, 72 more genes
    nsv4228539copy number variation1nstd166human GRCh37.p13 chr14: 76,122,157-76,122,253 , GRCh38.p12 chr14: 75,655,814-75,655,910 ERG28
    nsv4218030copy number variation1nstd166human GRCh37.p13 chr14: 76,118,156-76,118,465 , GRCh38.p12 chr14: 75,651,813-75,652,122 ERG28
    nsv4212664copy number variation1nstd166human GRCh37.p13 chr14: 76,127,672-76,127,856 , GRCh38.p12 chr14: 75,661,329-75,661,513 TTLL5, ERG28
    nsv3955687copy number variation1nstd168human GRCh38 chr14: 75,624,632-75,652,025 , GRCh37.p13 chr14: 76,090,975-76,118,368 ERG28, FLVCR2
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