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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
    nsv5154643mobile element insertion1nstd203human GRCh38 chr14: 64,913,660-64,913,675 , GRCh37.p13 chr14: 65,380,378-65,380,393 CHURC1, CHURC1-FNTB
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv4729599copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 61,409,856-65,742,610 , GRCh38.p12 chr14: 60,943,138-65,275,892 PARP1P2, ESR2, 73 more genes
    nsv4578028mobile element insertion1nstd166human GRCh37.p13 chr14: 65,379,227-65,379,227 , GRCh38.p12 chr14: 64,912,509-64,912,509 CHURC1, CHURC1-FNTB
    nsv4515394mobile element insertion1nstd166human GRCh37.p13 chr14: 65,394,137-65,394,137 , GRCh38.p12 chr14: 64,927,419-64,927,419 CHURC1, CHURC1-FNTB
    nsv4340065sequence alteration1nstd166human GRCh37.p13 chr14: 63,501,085-66,409,469 , GRCh38.p12 chr14: 63,034,367-65,942,751 , FUT8, 60 more genes
    nsv4229194copy number variation1nstd166human GRCh37.p13 chr14: 65,397,396-65,397,470 , GRCh38.p12 chr14: 64,930,678-64,930,752 CHURC1, CHURC1-FNTB
    nsv4217928copy number variation1nstd166human GRCh37.p13 chr14: 65,384,292-65,384,363 , GRCh38.p12 chr14: 64,917,574-64,917,645 CHURC1, CHURC1-FNTB
    nsv3963799copy number variation1nstd168human GRCh38 chr14: 64,841,504-64,930,168 , GRCh37.p13 chr14: 65,308,222-65,396,886 RPPH1-2P, SPTB, 3 more genes
    nsv3923965copy number variation1nstd102humanPathogenic GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803 ESR2, PPP2R5E, 111 more genes
    nsv3922652copy number variation1nstd102humanPathogenic GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231 PARP1P2, SNAPC1, 160 more genes
    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
    nsv3912530copy number variation1nstd102humanPathogenic NCBI36 chr14: 61,789,171-65,289,887 , GRCh38 chr14: 62,252,700-65,753,416 , GRCh37 chr14: 62,719,418-66,220,134 MIR625, LINC02324, 59 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
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