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 192

    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
    nsv7064476inversion1nstd229human GRCh38 chr11: 123,462,060-125,907,500 , GRCh37.p13 chr11: 123,332,768-125,777,395 STT3A, OR8G1, 101 more genes
    nsv6916077copy number variation1nstd229human GRCh38 chr11: 124,575,701-124,974,400 , GRCh37.p13 chr11: 124,445,597-124,844,296 SIAE, HEPACAM, 19 more genes
    nsv6912886copy number variation1nstd229human GRCh38 chr11: 124,629,263-124,634,571 , GRCh37.p13 chr11: 124,499,159-124,504,467 RNA5SP352, SIAE, 1 more genes
    nsv6907856copy number variation1nstd229human GRCh38 chr11: 124,539,858-124,705,388 , GRCh37.p13 chr11: 124,409,754-124,575,284 OR8Q1P, TBRG1, 6 more genes
    nsv6898203copy number variation1nstd229human GRCh38 chr11: 124,631,297-124,631,484 , GRCh37.p13 chr11: 124,501,193-124,501,380 SIAE, TBRG1
    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
    nsv6463888copy number variation1nstd223human GRCh38 chr11: 124,539,858-124,705,383 , GRCh37.p13 chr11: 124,409,754-124,575,279 SPA17, SIAE, 6 more genes
    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
    nsv6309036copy number variation3nstd102humanUncertain significance GRCh37 chr11: 123,504,851-126,163,012 , GRCh38.p12 chr11: 123,634,143-126,293,117 CDON, PKNOX2-DT, 113 more genes
    nsv6292022mobile element insertion1nstd186human GRCh37 chr11: 124,499,940-124,499,991 , GRCh38.p12 chr11: 124,630,044-124,630,095 TBRG1
    nsv6291285copy number variation1nstd102humanUncertain significance GRCh37 chr11: 124,296,335-124,560,100 , GRCh38.p12 chr11: 124,426,439-124,690,204 OR8B8, SPA17, 12 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
    nsv6258444mobile element insertion1nstd215human GRCh38 chr11: 124,630,044-124,630,044 , GRCh37.p13 chr11: 124,499,940-124,499,940 TBRG1
    nsv6131839copy number variation1nstd213human GRCh37 chr11: 124,350,000-124,620,001 , GRCh38.p12 chr11: 124,480,104-124,750,105 OR8B9P, TBRG1, 13 more genes
    nsv5706228mobile element insertion2nstd211human GRCh38 chr11: 124,630,044-124,630,044 , GRCh37.p13 chr11: 124,499,940-124,499,940 TBRG1
    nsv5429702mobile element insertion1nstd206human GRCh38 chr11: 124,630,044-124,630,095 , GRCh37.p13 chr11: 124,499,940-124,499,991 TBRG1
    nsv5134495mobile element insertion1nstd203human GRCh38 chr11: 124,630,081-124,630,084 , GRCh37.p13 chr11: 124,499,977-124,499,980 TBRG1
    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