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 223

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137129copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,531,028-134,257,553 , GRCh38.p12 chr11: 120,660,319-134,387,659 VSIG10L2, OR8B6P, 268 more genes
    nsv7077728inversion1nstd229human GRCh38 chr11: 124,239,803-134,089,458 , GRCh37.p13 chr11: 124,110,545-133,959,353 LOC283172, PPP1R10P1, 175 more genes
    nsv7069138inversion1nstd229human GRCh38 chr11: 128,470,446-128,811,017 , GRCh37.p13 chr11: 128,340,341-128,680,912 SENCR, LOC101929538, 6 more genes
    nsv6912557copy number variation1nstd229human GRCh38 chr11: 128,683,527-128,686,820 , GRCh37.p13 chr11: 128,553,422-128,556,715 FLI1, LOC101929538
    nsv6912205copy number variation1nstd229human GRCh38 chr11: 128,538,001-129,014,800 , GRCh37.p13 chr11: 128,407,896-128,884,695 KCNJ1, KCNJ5-AS1, 11 more genes
    nsv6637558copy number variation1nstd102humanPathogenic GRCh37 chr11: 122,975,824-134,938,470 , GRCh38.p12 chr11: 123,105,116-135,068,576 OR8B8, LOC107984373, 234 more genes
    nsv6634467copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 127,074,235-135,006,516 , GRCh38.p12 chr11: 127,204,340-135,076,622 APLP2, BAK1P2, 98 more genes
    nsv6465485copy number variation1nstd223human GRCh38 chr11: 128,683,732-128,684,220 , GRCh37.p13 chr11: 128,553,627-128,554,115 FLI1, LOC101929538
    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
    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
    nsv6132083copy number variation1nstd213human GRCh37 chr11: 126,840,000-128,920,001 , GRCh38.p12 chr11: 126,970,104-129,050,106 ETS1, KCNJ1, 28 more genes
    nsv4981265copy number variation1nstd200human GRCh38 chr11: 128,686,430-128,687,029 , GRCh37.p13 chr11: 128,556,325-128,556,924 FLI1, LOC101929538
    nsv4732750copy number variation1nstd199human GRCh37 chr11: 114,433,314-131,230,467 , GRCh38.p12 chr11: 114,562,592-131,360,572 , LINC02702, 392 more genes
    nsv4729012copy number variation1nstd102humanPathogenic GRCh37 chr11: 127,602,115-134,938,470 , GRCh38.p12 chr11: 127,732,220-135,068,576 LINC02706, APLP2, 92 more genes
    nsv4728891copy number variation1nstd102humanPathogenic GRCh37 chr11: 125,785,487-134,938,470 , GRCh38.p12 chr11: 125,915,592-135,068,576 ARHGAP32, NAP1L1P1, 125 more genes
    nsv4675832copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,742,540-134,938,470 , GRCh38.p12 chr11: 120,871,831-135,068,576 MIR8052, BLID, 275 more genes
    nsv4675703copy number variation1nstd102humanUncertain significance GRCh37 chr11: 128,194,490-128,595,064 , GRCh38.p12 chr11: 128,324,595-128,725,169 FLI1, SENCR, 6 more genes
    nsv4675674copy number variation1nstd102humanPathogenic GRCh37 chr11: 124,232,608-134,938,470 , GRCh38.p12 chr11: 124,362,712-135,068,576 FAM118B, PUS3, 184 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
    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