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 119

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093833copy number variation6nstd102humanUncertain significance GRCh37 chr11: 116,691,583-121,500,272 , GRCh38.p12 chr11: 116,820,867-121,629,563 RN7SL688P, MIR4492, 131 more genes
    nsv7093757copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,103,138-121,060,609 , GRCh38.p12 chr11: 119,232,428-121,189,900 USP2-AS1, LOC101929208, 41 more genes
    nsv7093753copy number variation1nstd102humanUncertain significance GRCh37 chr11: 117,209,303-120,133,495 , GRCh38.p12 chr11: 117,338,587-120,262,786 TMEM25, HYOU1, 93 more genes
    nsv7074550inversion1nstd229human GRCh38 chr11: 118,332,309-119,477,352 , GRCh37.p13 chr11: 118,203,024-119,348,063 VPS11, LOC100131626, 55 more genes
    nsv7062420inversion1nstd229human GRCh38 chr11: 117,681,463-119,526,734 , GRCh37.p13 chr11: 117,552,178-119,397,444 RN7SL688P, MIR4492, 72 more genes
    nsv6915386copy number variation1nstd229human GRCh38 chr11: 119,422,686-119,503,648 , GRCh37.p13 chr11: 119,293,396-119,374,359 USP2-AS1, DUXAP5, 1 more genes
    nsv6914602copy number variation1nstd229human GRCh38 chr11: 119,292,683-119,545,665 , GRCh37.p13 chr11: 119,163,393-119,416,375 MIR6756, RNF26, 9 more genes
    nsv6904372copy number variation1nstd229human GRCh38 chr11: 119,422,201-119,436,900 , GRCh37.p13 chr11: 119,292,911-119,307,610 USP2-AS1, THY1
    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
    nsv6308962copy number variation1nstd102humanUncertain significance GRCh37 chr11: 116,660,844-121,500,272 , GRCh38.p12 chr11: 116,790,128-121,629,563 LOC107984399, PCSK7, 132 more genes
    nsv6291074copy number variation1nstd102humanPathogenic GRCh37 chr11: 112,375,478-128,785,742 , GRCh38.p12 chr11: 112,504,755-128,915,847 ZW10, MPZL2, 378 more genes
    nsv6289927copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,288,964-134,937,416 , GRCh38.p12 chr11: 104,418,236-135,067,522 IGSF9B, MIR10526, 592 more genes
    nsv5925010copy number variation1nstd209human GRCh38 chr11: 119,417,464-119,417,519 , GRCh37.p13 chr11: 119,288,174-119,288,229 THY1, USP2-AS1
    nsv5380954copy number variation1nstd102humanUncertain significance GRCh37 chr11: 119,077,108-120,133,495 , GRCh38.p12 chr11: 119,206,398-120,262,786 NECTIN1-DT, RNU6-262P, 29 more genes
    nsv5348353translocation1nstd200human GRCh38 chr11: 119,417,466-119,417,466 , GRCh38 chr11: 119,417,520-119,417,520 , GRCh37.p13 chr11: 119,288,176-119,288,176 , GRCh37.p13 chr11: 119,288,230-119,288,230 USP2-AS1, THY1
    nsv4989363copy number variation1nstd200human GRCh38 chr11: 119,422,219-119,436,897 , GRCh37.p13 chr11: 119,292,929-119,307,607 THY1, USP2-AS1
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4675236copy number variation1nstd102humanUncertain significance GRCh37 chr11: 118,280,670-119,650,105 , GRCh38.p12 chr11: 118,409,955-119,779,396 SETP16, UPK2, 59 more genes
    nsv4674572copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 114,433,313-131,230,466 , GRCh38.p12 chr11: 114,562,591-131,360,571 ACRV1, APLP2, 382 more genes
    nsv4455281copy number variation1nstd102humanPathogenic GRCh37 chr11: 117,830,263-134,938,470 , GRCh38.p12 chr11: 117,959,548-135,068,576 NTM-AS1, LOC403312, 369 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