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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
    nsv5316877copy number variation1nstd204human GRCh38.p13 chr14: 64,064,368-64,316,268 , GRCh37.p13 chr14: 64,531,086-64,782,986 ESR2, MIR548H1, 1 more genes
    nsv5273870copy number variation1nstd204human GRCh38.p13 chr14: 64,064,227-64,105,804 , GRCh37.p13 chr14: 64,530,945-64,572,522 MIR548H1, SYNE2
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004688copy number variation1nstd200human GRCh38 chr14: 64,064,378-64,316,260 , GRCh37.p13 chr14: 64,531,096-64,782,978 SYNE2, ESR2, 1 more genes
    nsv4844739copy number variation1nstd200human GRCh37 chr14: 64,531,096-64,782,978 , GRCh38.p12 chr14: 64,064,378-64,316,260 SYNE2, ESR2, 1 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
    nsv4728880copy number variation1nstd102humanUncertain significance GRCh37 chr14: 64,399,555-64,748,326 , GRCh38.p12 chr14: 63,932,837-64,281,608 SYNE2, ESR2, 1 more genes
    nsv4383303copy number variation1nstd173human GRCh37 chr14: 64,060,740-64,743,107 , GRCh38.p12 chr14: 63,594,022-64,276,389 LOC105370532, RNU6-597P, 12 more genes
    nsv4340065sequence alteration1nstd166human GRCh37.p13 chr14: 63,501,085-66,409,469 , GRCh38.p12 chr14: 63,034,367-65,942,751 , FUT8, 60 more genes
    nsv3924033copy number variation1nstd102humanPathogenic GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999 DACT1, UBA52P3, 105 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
    nsv3922280copy number variation1nstd102humanUncertain significance NCBI36 chr14: 62,690,193-63,630,122 , GRCh38 chr14: 63,153,722-64,093,651 , GRCh37 chr14: 63,620,440-64,560,369 PPP2R5E, LOC105370531, 18 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
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