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 432

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145678insertion1nstd232human GRCh37.p13 chr14: 50,929,496-50,929,496 , GRCh38.p12 chr14: 50,462,778-50,462,778 MAP4K5
    nsv7094255copy number variation1nstd102humanUncertain significance GRCh37 chr14: 51,026,984-51,099,057 , GRCh38.p12 chr14: 50,560,266-50,632,339 MAP4K5, SNRPGP1, 2 more genes
    nsv7076302inversion1nstd229human GRCh38 chr14: 46,512,743-51,785,975 , GRCh37.p13 chr14: 46,981,946-52,252,693 LOC100420098, MAP4K5, 82 more genes
    nsv7069774inversion1nstd229human GRCh38 chr14: 50,509,662-51,212,481 , GRCh37.p13 chr14: 50,976,380-51,679,199 MRPL57P9, ABHD12B, 11 more genes
    nsv7063700inversion1nstd229human GRCh38 chr14: 48,591,726-55,698,685 , GRCh37.p13 chr14: 49,060,929-56,165,403 ZFP64P1, LINC02331, 132 more genes
    nsv7059488inversion1nstd229human GRCh38 chr14: 50,522,537-50,522,650 , GRCh37.p13 chr14: 50,989,255-50,989,368 MAP4K5
    nsv7059291inversion1nstd229human GRCh38 chr14: 49,838,942-56,572,993 , GRCh37.p13 chr14: 50,305,660-57,039,711 LOC105370500, LINC01599, 124 more genes
    nsv6957695copy number variation1nstd229human GRCh38 chr14: 50,560,907-50,572,541 , GRCh37.p13 chr14: 51,027,625-51,039,259 SNRPGP1, ATL1, 1 more genes
    nsv6957482copy number variation1nstd229human GRCh38 chr14: 50,526,662-50,531,887 , GRCh37.p13 chr14: 50,993,380-50,998,605 ATL1, MAP4K5
    nsv6957235copy number variation1nstd229human GRCh38 chr14: 50,489,542-50,489,744 , GRCh37.p13 chr14: 50,956,260-50,956,462 MAP4K5
    nsv6956473copy number variation1nstd229human GRCh38 chr14: 50,414,969-50,417,239 , GRCh37.p13 chr14: 50,881,687-50,883,957 MAP4K5
    nsv6956013copy number variation1nstd229human GRCh38 chr14: 50,551,557-50,559,150 , GRCh37.p13 chr14: 51,018,275-51,025,868 ATL1, MAP4K5
    nsv6953062copy number variation1nstd229human GRCh38 chr14: 50,506,533-50,509,589 , GRCh37.p13 chr14: 50,973,251-50,976,307 MAP4K5
    nsv6950089copy number variation1nstd229human GRCh38 chr14: 50,550,514-50,556,798 , GRCh37.p13 chr14: 51,017,232-51,023,516 MAP4K5, ATL1
    nsv6949096copy number variation1nstd229human GRCh38 chr14: 50,393,346-50,501,997 , GRCh37.p13 chr14: 50,860,064-50,968,715 CDKL1, LOC100419913, 1 more genes
    nsv6946065copy number variation1nstd229human GRCh38 chr14: 50,506,653-51,212,480 , GRCh37.p13 chr14: 50,973,371-51,679,198 PYGL, MAP4K5, 11 more genes
    nsv6945659copy number variation1nstd229human GRCh38 chr14: 50,494,706-50,498,549 , GRCh37.p13 chr14: 50,961,424-50,965,267 MAP4K5
    nsv6945124copy number variation1nstd229human GRCh38 chr14: 50,537,001-50,550,200 , GRCh37.p13 chr14: 51,003,719-51,016,918 ATL1, MAP4K5
    nsv6944713copy number variation1nstd229human GRCh38 chr14: 50,492,854-50,501,581 , GRCh37.p13 chr14: 50,959,572-50,968,299 MAP4K5
    nsv6942423copy number variation1nstd229human GRCh38 chr14: 50,487,573-50,494,181 , GRCh37.p13 chr14: 50,954,291-50,960,899 MAP4K5
    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