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 209

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5005044copy number variation1nstd200human GRCh38 chr14: 104,918,223-105,014,223 , GRCh37.p13 chr14: 105,384,560-105,480,560 CDCA4, AHNAK2, 2 more genes
    nsv4991615copy number variation1nstd200human GRCh38 chr14: 104,961,321-105,004,766 , GRCh37.p13 chr14: 105,427,658-105,471,103 AHNAK2, CLBA1
    nsv4991604copy number variation1nstd200human GRCh38 chr14: 104,936,399-105,157,927 , GRCh37.p13 chr14: 105,402,736-105,624,264 JAG2, GPR132, 6 more genes
    nsv4729218copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,615,953-107,285,437 , GRCh38.p12 chr14: 102,149,616-106,877,229 IGHV4-61, IGHD3-9, 308 more genes
    nsv4728966copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,204,147-105,543,486 , GRCh38.p12 chr14: 104,737,810-105,077,149 CLBA1, ZBTB42, 15 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4675524copy number variation1nstd102humanPathogenic GRCh37 chr14: 104,764,078-107,285,437 , GRCh38.p12 chr14: 104,297,741-106,877,229 IGHV3-76, IGHV5-10-1, 241 more genes
    nsv4675364copy number variation1nstd102humanPathogenic GRCh37 chr14: 105,303,584-107,285,437 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 , GRCh38.p12 chr14: 104,837,247-106,877,229 PACS2, IGHVII-15-1, 226 more genes
    nsv4624902copy number variation1nstd183human GRCh37 chr14: 103,676,460-105,831,463 , GRCh38.p12 chr14: 103,210,123-105,365,126 , ZFYVE21, 69 more genes
    nsv4624595copy number variation1nstd183human GRCh37 chr14: 104,929,882-106,342,979 , GRCh38.p12 chr14: 104,466,471-105,877,120 , IGHJ2, 73 more genes
    nsv4530111copy number variation1nstd166human GRCh37.p13 chr14: 105,429,999-105,577,000 , GRCh38.p12 chr14: 104,963,662-105,110,663 AHNAK2, CDCA4, 3 more genes
    nsv4456944copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,627,916-107,147,698 , GRCh38.p12 chr14: 101,161,579-106,691,681 IGHV1-58, IGHVII-60-1, 308 more genes
    nsv4456320copy number variation1nstd102humanPathogenic GRCh37 chr14: 102,931,119-107,285,437 , GRCh38.p12 chr14: 102,464,782-106,877,229 LOC105378184, LINC02298, 302 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455831copy number variation1nstd102humanUncertain significance GRCh37 chr14: 105,067,651-107,285,437 , GRCh38.p12 chr14|NT_187600.1: 1-1,214,078 , GRCh38.p12 chr14: 104,622,881-106,877,229 VESTAR, IGHVIII-25-1, 238 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
    nsv4436056complex substitution1nstd102humanUncertain significance GRCh38.p12 chr14: 104,177,384-105,466,438 , GRCh37 chr14: 104,643,721-105,932,775 AKT1, BRF1, 35 more genes
    nsv4427704copy number variation1nstd174human GRCh37 chr14: 105,423,761-105,722,653 , GRCh38.p12 chr14: 104,957,424-105,256,316 GPR132, LINC02298, 8 more genes
    nsv4350091copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 103,804,791-105,677,579 , GRCh38.p12 chr14: 103,338,454-105,211,242 AKT1, CKB, 58 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