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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094439copy number variation2nstd102humanUncertain significance GRCh37 chr14: 60,976,117-61,447,691 , GRCh38.p12 chr14: 60,509,399-60,980,973 MAD2L1P1, SLC38A6, 12 more genes
    nsv7078008inversion1nstd229human GRCh38 chr14: 60,214,891-67,756,686 , GRCh37.p13 chr14: 60,681,609-68,223,403 ATP6V1D, LOC101927756, 129 more genes
    nsv7074395inversion1nstd229human GRCh38 chr14: 60,340,053-62,327,269 , GRCh37.p13 chr14: 60,806,771-62,793,987 MAD2L1P1, GNRHR2P1, 33 more genes
    nsv7060471inversion1nstd229human GRCh38 chr14: 54,671,401-63,742,041 , GRCh37.p13 chr14: 55,138,119-64,208,759 KTN1, OTX2-AS1, 153 more genes
    nsv6954502copy number variation1nstd229human GRCh38 chr14: 60,649,492-60,652,908 , GRCh37.p13 chr14: 61,116,210-61,119,626 SIX1
    nsv6952769copy number variation1nstd229human GRCh38 chr14: 60,626,077-60,665,388 , GRCh37.p13 chr14: 61,092,795-61,132,106 MIR9718, SALRNA1, 1 more genes
    nsv6952443copy number variation1nstd229human GRCh38 chr14: 57,104,906-61,096,631 , GRCh37.p13 chr14: 57,571,624-61,563,349 LRRC9, RTN1, 71 more genes
    nsv6949011copy number variation1nstd229human GRCh38 chr14: 57,104,849-61,096,728 , GRCh37.p13 chr14: 57,571,567-61,563,446 MAD2L1P1, AP5M1, 71 more genes
    nsv6947825copy number variation1nstd229human GRCh38 chr14: 60,642,713-60,738,304 , GRCh37.p13 chr14: 61,109,431-61,205,022 SIX1, MNAT1, 2 more genes
    nsv6637682copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485 PARP1P2, HIF1A, 91 more genes
    nsv6594267inversion1nstd223human GRCh38 chr14: 54,883,431-63,921,497 , GRCh37.p13 chr14: 55,350,149-64,388,215 RPL36AP1, GNRHR2P1, 152 more genes
    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
    nsv6291507copy number variation1nstd102humanUncertain significance GRCh37 chr14: 60,958,879-61,211,351 , GRCh38.p12 chr14: 60,492,161-60,744,633 SALRNA1, MIR9718, 9 more genes
    nsv6132790copy number variation2nstd213human GRCh37 chr14: 61,000,000-61,870,001 , GRCh38.p12 chr14: 60,533,282-61,403,283 MNAT1, PRKCH, 14 more genes
    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
    nsv5380830copy number variation1nstd102humanUncertain significance GRCh37 chr14: 60,976,117-61,191,013 , GRCh38.p12 chr14: 60,509,399-60,724,295 MIR9718, RPL37P5, 6 more genes
    nsv5264058copy number variation1nstd204human GRCh38.p13 chr14: 60,605,501-61,055,200 , GRCh37.p13 chr14: 61,072,219-61,521,918 RNU6-398P, SRMP2, 9 more genes
    nsv5261677copy number variation1nstd204human GRCh38.p13 chr14: 60,647,203-60,692,125 , GRCh37.p13 chr14: 61,113,921-61,158,843 MIR9718, SIX1
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4999589copy number variation1nstd200human GRCh38 chr14: 60,649,614-60,649,675 , GRCh37.p13 chr14: 61,116,332-61,116,393 SIX1
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