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 745

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077384inversion1nstd229human GRCh38 chr11: 36,117,438-36,119,187 , GRCh37.p13 chr11: 36,138,988-36,140,737 LDLRAD3
    nsv7077310inversion1nstd229human GRCh38 chr11: 36,116,388-36,119,187 , GRCh37.p13 chr11: 36,137,938-36,140,737 LDLRAD3
    nsv7066211inversion1nstd229human GRCh38 chr11: 36,038,110-36,038,167 , GRCh37.p13 chr11: 36,059,660-36,059,717 LDLRAD3
    nsv7065886inversion1nstd229human GRCh38 chr11: 36,181,478-36,190,589 , GRCh37.p13 chr11: 36,203,028-36,212,139 LDLRAD3
    nsv7060843inversion1nstd229human GRCh38 chr11: 35,998,044-35,998,066 , GRCh37.p13 chr11: 36,019,594-36,019,616 RPL12P31, LDLRAD3
    nsv6916823copy number variation1nstd229human GRCh38 chr11: 35,941,896-35,942,018 , GRCh37.p13 chr11: 35,963,446-35,963,568 LDLRAD3
    nsv6915738copy number variation1nstd229human GRCh38 chr11: 35,968,770-35,976,103 , GRCh37.p13 chr11: 35,990,320-35,997,653 WEE2P1, LDLRAD3
    nsv6913781copy number variation1nstd229human GRCh38 chr11: 34,168,221-36,836,658 , GRCh37.p13 chr11: 34,189,768-36,858,208 TRAF6, LOC100422241, 39 more genes
    nsv6913573copy number variation1nstd229human GRCh38 chr11: 35,843,396-36,019,641 , GRCh37.p13 chr11: 35,864,946-36,041,191 WEE2P1, MIR3973, 3 more genes
    nsv6913461copy number variation1nstd229human GRCh38 chr11: 36,200,200-36,302,574 , GRCh37.p13 chr11: 36,221,750-36,324,124 COMMD9, PRR5L, 1 more genes
    nsv6912515copy number variation1nstd229human GRCh38 chr11: 35,765,791-36,021,646 , GRCh37.p13 chr11: 35,787,340-36,043,196 TRIM44, KRT18P14, 4 more genes
    nsv6912399copy number variation1nstd229human GRCh38 chr11: 36,003,125-36,006,639 , GRCh37.p13 chr11: 36,024,675-36,028,189 LDLRAD3
    nsv6912234copy number variation1nstd229human GRCh38 chr11: 36,101,660-36,105,396 , GRCh37.p13 chr11: 36,123,210-36,126,946 LDLRAD3
    nsv6909590copy number variation1nstd229human GRCh38 chr11: 36,183,301-36,188,900 , GRCh37.p13 chr11: 36,204,851-36,210,450 LDLRAD3
    nsv6909302copy number variation1nstd229human GRCh38 chr11: 36,192,001-36,212,600 , GRCh37.p13 chr11: 36,213,551-36,234,150 LDLRAD3
    nsv6909082copy number variation1nstd229human GRCh38 chr11: 36,138,769-36,142,744 , GRCh37.p13 chr11: 36,160,319-36,164,294 LDLRAD3
    nsv6908851copy number variation1nstd229human GRCh38 chr11: 36,170,231-36,170,306 , GRCh37.p13 chr11: 36,191,781-36,191,856 LDLRAD3
    nsv6908338copy number variation1nstd229human GRCh38 chr11: 36,116,633-36,117,440 , GRCh37.p13 chr11: 36,138,183-36,138,990 LDLRAD3
    nsv6908237copy number variation1nstd229human GRCh38 chr11: 36,084,616-36,088,038 , GRCh37.p13 chr11: 36,106,166-36,109,588 LDLRAD3
    nsv6907661copy number variation1nstd229human GRCh38 chr11: 35,988,128-35,992,465 , GRCh37.p13 chr11: 36,009,678-36,014,015 LDLRAD3
    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