U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 71

    loading data ...

    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
    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
    nsv4340065sequence alteration1nstd166human GRCh37.p13 chr14: 63,501,085-66,409,469 , GRCh38.p12 chr14: 63,034,367-65,942,751 , FUT8, 60 more genes
    nsv3962447copy number variation1nstd168human GRCh38 chr14: 65,041,081-65,079,302 , GRCh37.p13 chr14: 65,507,799-65,546,020 FNTB, MAX, 2 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
    nsv3919866copy number variation1nstd102humanUncertain significance NCBI36 chr14: 64,489,394-65,831,760 , GRCh37 chr14: 65,419,641-66,762,007 , GRCh38 chr14: 64,952,923-66,295,289 FTH1P13, PTBP1P, 22 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
    nsv3168616copy number variation1nstd158human GRCh38.p12 chr14: 63,156,948-86,570,963 , GRCh37 chr14: 63,623,666-87,037,307 , ACTN1, 394 more genes
    nsv3155299copy number variation1nstd151human GRCh37 chr14: 65,289,662-65,560,538 , GRCh38.p12 chr14: 64,822,944-65,093,820 MIR4706, LOC105370534, 10 more genes
    nsv3153883copy number variation1nstd151human GRCh37 chr14: 65,453,669-65,569,062 , GRCh38.p12 chr14: 64,986,951-65,102,344 FNTB, MAX, 4 more genes
    nsv3150881copy number variation1nstd151human GRCh37 chr14: 65,271,654-65,560,538 , GRCh38.p12 chr14: 64,804,936-65,093,820 LOC107984655, LOC100506321, 10 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center