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Items: 1 to 20 of 122

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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
    nsv5938835copy number variation1nstd209human GRCh38 chr14: 50,842,894-59,394,609 , GRCh37.p13 chr14: 51,309,612-59,861,327 , TMX1, 148 more genes
    nsv5933734copy number variation1nstd209human GRCh38 chr14: 55,143,843-55,143,906 , GRCh37.p13 chr14: 55,610,561-55,610,624 LGALS3
    nsv5932908copy number variation1nstd209human GRCh38 chr14: 54,986,990-55,337,950 , GRCh37.p13 chr14: 55,453,708-55,804,668 LOC107984708, SOCS4, 12 more genes
    nsv5654378insertion1nstd207human GRCh38 chr14: 55,143,843-55,143,843 , GRCh37.p13 chr14: 55,610,561-55,610,561 LGALS3
    nsv5555347sequence alteration1nstd206human GRCh38 chr14: 54,915,499-55,646,544 , GRCh37.p13 chr14: 55,382,217-56,113,262 , ATG14, 21 more genes
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4498573mobile element insertion1nstd166human GRCh37.p13 chr14: 55,607,510-55,607,510 , GRCh38.p12 chr14: 55,140,792-55,140,792 LGALS3
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 SRMP2, IGHV3-71, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 MIR656, TRAJ59, 1918 more genes
    nsv3916278copy number variation1nstd102humanPathogenic GRCh38 chr14: 50,591,011-56,286,919 , GRCh37 chr14: 51,057,729-56,753,637 , NCBI36 chr14: 50,127,479-55,823,390 LOC105370507, ATG14, 98 more genes
    nsv3913833copy number variation1nstd102humanPathogenic NCBI36 chr14: 51,081,314-54,857,069 , GRCh38 chr14: 51,544,846-55,320,598 , GRCh37 chr14: 52,011,564-55,787,316 SOCS4, FRMD6, 65 more genes
    nsv3911849copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 38,735,127-56,250,932 , GRCh37 chr14: 39,665,376-57,181,179 , GRCh38 chr14: 39,196,172-56,714,461 ARF6, BMP4, 219 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 BANF1P1, IGHV1-68, 1996 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 CRIP1, GPATCH2L, 1929 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 DHRS7, MIR548Y, 1946 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 LOC440181, HEATR5A-DT, 1998 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 LOC100289511, RNU6-552P, 1996 more genes
    nsv3893887copy number variation1nstd102humanUncertain significance GRCh37 chr14: 54,530,302-55,812,050 , GRCh38.p12 chr14: 54,063,584-55,345,332 DLGAP5, MIR4308, 25 more genes
    nsv3891643copy number variation1nstd102humanBenign GRCh37 chr14: 55,440,068-55,655,692 , GRCh38.p12 chr14: 54,973,350-55,188,974 RPSAP13, DLGAP5, 4 more genes
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