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 122

    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
    nsv7065486inversion1nstd229human GRCh38 chr11: 65,309,443-65,482,021 , GRCh37.p13 chr11: 65,076,914-65,249,492 CDC42EP2, NEAT1, 7 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
    nsv6908118copy number variation1nstd229human GRCh38 chr11: 65,433,980-65,448,399 , GRCh37.p13 chr11: 65,201,451-65,215,870 NEAT1, MIR612
    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
    nsv6900053copy number variation1nstd229human GRCh38 chr11: 65,436,493-65,443,578 , GRCh37.p13 chr11: 65,203,964-65,211,049 MIR612, NEAT1
    nsv6466420copy number variation1nstd223human GRCh38 chr11: 65,436,492-65,443,577 , GRCh37.p13 chr11: 65,203,963-65,211,048 NEAT1, MIR612
    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
    nsv6309121copy number variation2nstd102humanPathogenic GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223 SF3B2, ZNRD2-DT, 124 more genes
    nsv6301259copy number variation1nstd186human GRCh37 chr11: 65,203,963-65,211,048 , GRCh38.p12 chr11: 65,436,492-65,443,577 NEAT1, MIR612
    nsv6132269copy number variation1nstd213human GRCh37 chr11: 64,390,000-65,950,001 , GRCh38.p12 chr11: 64,622,528-66,182,530 MRPL49, CTSW, 103 more genes
    nsv6132112copy number variation1nstd213human GRCh37 chr11: 64,220,000-68,010,001 , GRCh38.p12 chr11: 64,452,528-68,242,533 ACTN3, ALDH3B1, 212 more genes
    nsv5505132copy number variation1nstd206human GRCh38 chr11: 65,436,492-65,443,577 , GRCh37.p13 chr11: 65,203,963-65,211,048 MIR612, NEAT1
    nsv5504342copy number variation1nstd206human GRCh38 chr11: 65,443,914-65,444,098 , GRCh37.p13 chr11: 65,211,385-65,211,569 NEAT1, MIR612
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5267852copy number variation1nstd204human GRCh38.p13 chr11: 64,173,401-65,676,300 , GRCh37.p13 chr11: 63,940,873-65,443,771 , TALAM1, 103 more genes
    nsv5262374copy number variation1nstd204human GRCh38.p13 chr11: 65,373,701-65,675,900 , GRCh37.p13 chr11: 65,141,172-65,443,371 , MIR612, 23 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