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 86

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940619copy number variation1nstd209human GRCh38 chr14: 41,756,659-48,371,099 , GRCh37.p13 chr14: 42,225,862-48,840,302 LOC100418768, RNU6-297P, 53 more genes
    nsv4994299copy number variation1nstd200human GRCh38 chr14: 46,442,619-46,787,900 , GRCh37.p13 chr14: 46,911,822-47,257,103 LINC00871, LOC105370480, 2 more genes
    nsv4841808copy number variation1nstd200human GRCh37 chr14: 46,911,822-47,257,103 , GRCh38.p12 chr14: 46,442,619-46,787,900 LOC105370480, LINC00871, 2 more genes
    nsv4679684copy number variation1nstd189human GRCh37.p13 chr14: 46,710,360-47,198,406 , GRCh38.p12 chr14: 46,241,157-46,729,203 RPL10L, LINC00871, 2 more genes
    nsv4674919copy number variation1nstd102humanLikely benign GRCh37 chr14: 46,907,047-47,255,343 , GRCh38.p12 chr14: 46,437,844-46,786,140 LINC00871, LOC105370480, 2 more genes
    nsv4507679mobile element insertion1nstd166human GRCh37.p13 chr14: 47,118,804-47,118,804 , GRCh38.p12 chr14: 46,649,601-46,649,601 RPL10L, LOC105370481
    nsv4213534copy number variation1nstd166human GRCh37.p13 chr14: 46,170,198-47,254,506 , GRCh38.p12 chr14: 45,700,995-46,785,303 RPL10L, LINC00871, 5 more genes
    nsv3969147copy number variation1nstd168human GRCh38 chr14: 46,648,626-46,674,199 , GRCh37.p13 chr14: 47,117,829-47,143,402 RPL10L, LOC105370481
    nsv3924872copy number variation1nstd102humanUncertain significance NCBI36 chr14: 45,957,678-46,375,065 , GRCh37.p13 chr14: 46,887,928-47,305,315 , GRCh38.p12 chr14: 46,418,725-46,836,112 LOC105370480, LINC00871, 3 more genes
    nsv3922670copy number variation1nstd102humanUncertain significance NCBI36 chr14: 46,183,816-46,327,453 , GRCh37 chr14: 47,114,066-47,257,703 , GRCh38 chr14: 46,644,863-46,788,500 RPL10L, LOC105370481
    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
    nsv3916173copy number variation1nstd102humanPathogenic NCBI36 chr14: 33,118,898-48,418,573 , GRCh37.p13 chr14: 34,049,147-49,348,823 , GRCh38.p12 chr14: 33,579,941-48,879,620 TTC6, LOC105370449, 178 more genes
    nsv3913548copy number variation1nstd102humanUncertain significance NCBI36 chr14: 46,183,675-47,111,449 , GRCh37.p13 chr14: 47,113,925-48,041,699 , GRCh38.p12 chr14: 46,644,722-47,572,496 RPL10L, RPL13AP2, 4 more genes
    nsv3913204copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-49,111,245 , GRCh38 chr14: 20,043,513-48,642,042 , NCBI36 chr14: 19,581,512-48,180,995 SMARCE1P3, LOC100421646, 635 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
    nsv3910692copy number variation1nstd102humanUncertain significance GRCh37 chr14: 46,463,665-47,786,297 , GRCh38 chr14: 45,994,462-47,317,094 , NCBI36 chr14: 45,533,415-46,856,047 LINC00871, RPL13AP2, 5 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
    nsv3906671copy number variation1nstd102humanUncertain significance GRCh37 chr14: 46,845,461-47,128,671 , GRCh38.p12 chr14: 46,376,258-46,659,468 RPL10L, LOC105370481, 2 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
    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