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 123

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5264027copy number variation1nstd204human GRCh37.p13 chr11: 117,008,417-117,080,816 , GRCh38.p13 chr11: 117,137,701-117,210,100 PAFAH1B2, TAGLN, 4 more genes
    nsv5035338inversion1nstd200human GRCh38 chr11: 114,039,980-117,481,226 , GRCh37.p13 chr11: 113,910,702-117,351,941 , LINC02703, 56 more genes
    nsv4980875copy number variation1nstd200human GRCh38 chr11: 117,171,472-117,177,084 , GRCh37.p13 chr11: 117,042,188-117,047,800 SIDT2, PAFAH1B2
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 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
    nsv4349506copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,691,675-134,889,485 , GRCh38.p12 chr11: 116,820,959-135,019,591 LOC107984407, DCPS, 394 more genes
    nsv4349045copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,700,253-134,904,063 , GRCh38.p12 chr11: 116,829,537-135,034,169 MPZL3, ADAMTS8, 393 more genes
    nsv3957546copy number variation1nstd168human GRCh38 chr11: 117,182,041-117,195,130 , GRCh37.p13 chr11: 117,052,757-117,065,846 LOC100652768, SIDT2
    nsv3923375copy number variation1nstd102humanPathogenic GRCh37 chr11: 116,722,088-134,868,420 , NCBI36 chr11: 116,227,298-134,373,630 , GRCh38 chr11: 116,851,372-134,998,526 VPS26B, LOC105369531, 390 more genes
    nsv3922253copy number variation1nstd102humanPathogenic GRCh37 chr11: 100,219,331-134,910,140 , NCBI36 chr11: 99,724,541-134,415,350 , GRCh38 chr11: 100,348,599-135,040,246 RPS27P19, UBASH3B, 655 more genes
    nsv3916857copy number variation2nstd102humanPathogenic NCBI36 chr11: 116,227,321-134,373,617 , GRCh37 chr11: 116,722,111-134,868,407 , GRCh38 chr11: 116,851,395-134,998,513 RPUSD4, ELOCP22, 390 more genes
    nsv3914316copy number variation1nstd102humanPathogenic NCBI36 chr11: 115,812,352-117,422,156 , GRCh38 chr11: 116,436,425-118,046,231 , GRCh37 chr11: 116,307,142-117,916,946 LOC653303, BUD13, 31 more genes
    nsv3913230copy number variation1nstd102humanPathogenic GRCh38 chr11: 113,444,446-120,648,921 , NCBI36 chr11: 112,820,378-120,024,840 , GRCh37 chr11: 113,315,168-120,519,630 ARHGEF12, LOC105369526, 169 more genes
    nsv3912905copy number variation1nstd102humanPathogenic GRCh38 chr11: 112,864,326-131,189,315 , GRCh37 chr11: 112,832,130-131,059,210 , NCBI36 chr11: 112,240,259-130,564,420 SLC37A2, OR6X1, 416 more genes
    nsv3911830copy number variation1nstd102humanPathogenic NCBI36 chr11: 116,182,194-134,450,377 , GRCh37 chr11: 116,676,984-134,945,165 , GRCh38 chr11: 116,806,268-135,075,271 ACRV1, BMPR1AP2, 395 more genes
    nsv3911601copy number variation1nstd102humanUncertain significance NCBI36 chr11: 115,023,598-116,957,808 , GRCh37 chr11: 115,518,388-117,452,598 , GRCh38 chr11: 115,647,670-117,581,883 ZPR1, LOC653303, 32 more genes
    nsv3911440copy number variation1nstd102humanPathogenic NCBI36 chr11: 116,244,861-134,450,377 , GRCh37 chr11: 116,739,651-134,945,165 , GRCh38 chr11: 116,868,935-135,075,271 RN7SL688P, ARHGEF12, 391 more genes
    nsv3909122copy number variation1nstd102humanPathogenic GRCh37 chr11: 115,215,434-120,559,928 , GRCh38.p12 chr11: 115,344,715-120,689,219 LOC107984393, CENATAC-DT, 136 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 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