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 217

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094093copy number variation2nstd102humanUncertain significance GRCh37 chr11: 64,973,914-70,052,579 , GRCh38.p12 chr11: 65,206,443-70,206,473 B4GAT1, CHKA-DT, 208 more genes
    nsv7093933copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 65,325,080-65,639,825 , GRCh38.p12 chr11: 65,557,609-65,872,354 ZNRD2-DT, ZNRD2, 22 more genes
    nsv7062888inversion1nstd229human GRCh38 chr11: 65,331,143-66,048,384 , GRCh37.p13 chr11: 65,098,614-65,815,855 FAUP4, MAP3K11, 50 more genes
    nsv7061449inversion1nstd229human GRCh38 chr11: 65,331,281-66,115,058 , GRCh37.p13 chr11: 65,098,752-65,882,529 LOC100420020, LINC02736, 53 more genes
    nsv6917227copy number variation1nstd229human GRCh38 chr11: 65,821,424-65,841,587 , GRCh37.p13 chr11: 65,588,895-65,609,058 SNX32
    nsv6914921copy number variation1nstd229human GRCh38 chr11: 65,667,113-66,107,104 , GRCh37.p13 chr11: 65,434,584-65,874,575 SNX32, OVOL1, 28 more genes
    nsv6913473copy number variation1nstd229human GRCh38 chr11: 65,831,517-65,837,623 , GRCh37.p13 chr11: 65,598,988-65,605,094 SNX32
    nsv6912389copy number variation1nstd229human GRCh38 chr11: 65,604,598-65,954,847 , GRCh37.p13 chr11: 65,372,069-65,722,318 RNASEH2C, C11orf68, 24 more genes
    nsv6905877copy number variation1nstd229human GRCh38 chr11: 60,405,001-68,536,600 , GRCh37.p13 chr11: 60,172,474-68,304,068 INCENP, SNRPCP12, 409 more genes
    nsv6903095copy number variation1nstd229human GRCh38 chr11: 59,466,654-66,168,743 , GRCh37.p13 chr11: 59,234,127-65,936,214 LINC02724, TMEM132A, 342 more genes
    nsv6473488copy number variation1nstd223human GRCh38 chr11: 65,845,360-65,846,404 , GRCh37.p13 chr11: 65,612,831-65,613,875 SNX32
    nsv6471918copy number variation1nstd223human GRCh38 chr11: 65,821,424-65,841,587 , GRCh37.p13 chr11: 65,588,895-65,609,058 SNX32
    nsv6471058copy number variation1nstd223human GRCh38 chr11: 65,839,296-65,839,648 , GRCh37.p13 chr11: 65,606,767-65,607,119 SNX32
    nsv6470952copy number variation1nstd223human GRCh38 chr11: 65,841,634-65,845,689 , GRCh37.p13 chr11: 65,609,105-65,613,160 SNX32
    nsv6467925copy number variation1nstd223human GRCh38 chr11: 65,821,873-65,838,020 , GRCh37.p13 chr11: 65,589,344-65,605,491 SNX32
    nsv6465787copy number variation1nstd223human GRCh38 chr11: 65,841,670-65,843,157 , GRCh37.p13 chr11: 65,609,141-65,610,628 SNX32
    nsv6461817copy number variation1nstd223human GRCh38 chr11: 65,831,517-65,837,618 , GRCh37.p13 chr11: 65,598,988-65,605,089 SNX32
    nsv6456327copy number variation1nstd223human GRCh38 chr11: 65,846,517-65,847,746 , GRCh37.p13 chr11: 65,613,988-65,615,217 SNX32
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 PYGM, ATL3, 2125 more genes
    nsv6314192copy number variation1nstd102humanUncertain significance GRCh37 chr11: 64,935,724-66,405,514 , GRCh38.p12 chr11: 65,168,253-66,638,043 CNIH2, GAL3ST3, 95 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