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 101

    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
    nsv6914093copy number variation1nstd229human GRCh38 chr11: 66,282,766-66,295,500 , GRCh37.p13 chr11: 66,050,237-66,062,971 YIF1A, CNIH2, 1 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
    nsv6621258copy number variation1nstd224human GRCh37 chr11: 66,055,077-66,066,664 , GRCh38.p12 chr11: 66,287,606-66,299,193 YIF1A, TMEM151A
    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
    nsv6290938copy number variation1nstd102humanUncertain significance GRCh37 chr11: 65,963,737-66,581,485 , GRCh38.p12 chr11: 66,196,266-66,814,014 CCS, RN7SL12P, 38 more genes
    nsv6132271copy number variation1nstd213human GRCh37 chr11: 66,040,000-66,380,001 , GRCh38.p12 chr11: 66,272,529-66,612,530 BBS1, YIF1A, 24 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
    nsv6031209copy number variation1nstd212human GRCh37.p13 chr11: 66,023,643-66,066,070 , GRCh38 chr11: 66,256,172-66,298,599 YIF1A, KLC2, 6 more genes
    nsv5499986copy number variation1nstd206human GRCh38 chr11: 66,285,553-66,285,789 , GRCh37.p13 chr11: 66,053,024-66,053,260 YIF1A
    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
    nsv5277798copy number variation1nstd204human GRCh38.p13 chr11: 65,676,501-66,823,500 , GRCh37.p13 chr11: 65,443,972-66,590,971 , BBS1, 68 more genes
    nsv5265802copy number variation1nstd204human GRCh38.p13 chr11: 66,289,020-66,291,419 , GRCh37.p13 chr11: 66,056,491-66,058,890 YIF1A, TMEM151A
    nsv5198581mobile element insertion1nstd203human GRCh38 chr11: 66,286,454-66,286,462 , GRCh37.p13 chr11: 66,053,925-66,053,933 YIF1A
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4601136copy number variation1nstd183human GRCh37 chr11: 66,050,349-66,050,492 , GRCh38.p12 chr11: 66,282,878-66,283,021 CNIH2, YIF1A
    nsv4453555copy number variation1nstd102humanUncertain significance GRCh38 chr11: 65,866,431-66,347,555 , GRCh37 chr11: 65,633,902-66,115,026 CNIH2, YIF1A, 33 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