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 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5700545mobile element insertion2nstd211human GRCh38 chr11: 4,368,678-4,368,678 , GRCh37.p13 chr11: 4,389,908-4,389,908 OR52B4
    nsv5599132copy number variation1nstd207human GRCh38 chr11: 4,365,421-4,365,929 , GRCh37.p13 chr11: 4,386,651-4,387,159 OR52B4
    nsv5507349copy number variation1nstd206human GRCh38 chr11: 4,332,000-4,540,000 , GRCh37.p13 chr11: 4,353,230-4,561,230 OR52K1, OR52P2P, 8 more genes
    nsv5495057copy number variation1nstd206human GRCh38 chr11: 4,272,500-4,437,500 , GRCh37.p13 chr11: 4,293,730-4,458,730 TRIM21, OR52P2P, 7 more genes
    nsv5405289mobile element insertion1nstd206human GRCh38 chr11: 4,368,678-4,368,729 , GRCh37.p13 chr11: 4,389,908-4,389,959 OR52B4
    nsv5257152copy number variation1nstd204human GRCh38.p13 chr11: 4,360,019-4,416,043 , GRCh37.p13 chr11: 4,381,249-4,437,273 TRIM21, OR52B4, 1 more genes
    nsv5243714copy number variation1nstd204human GRCh38.p13 chr11: 4,217,901-4,523,400 , GRCh37.p13 chr11: 4,239,131-4,544,630 OR52K2, OR52M2P, 13 more genes
    nsv5139228mobile element insertion1nstd203human GRCh38 chr11: 4,368,662-4,368,678 , GRCh37.p13 chr11: 4,389,892-4,389,908 OR52B4
    nsv5122062mobile element insertion1nstd203human GRCh38 chr11: 4,368,665-4,368,678 , GRCh37.p13 chr11: 4,389,895-4,389,908 OR52B4
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    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
    nsv4729112copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-4,851,537 , GRCh38.p12 chr11: 230,615-4,830,307 OR51E1, TNNI2, 203 more genes
    nsv4729081copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,238,630-4,460,261 , GRCh38.p12 chr11: 4,217,400-4,439,031 SSU72L1, OR52B4, 9 more genes
    nsv4728922copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,388,904-4,639,840 , GRCh38.p12 chr11: 4,367,674-4,618,610 OR52K1, OR52B4, 12 more genes
    nsv4679088copy number variation1nstd189human GRCh37.p13 chr11: 4,335,879-4,833,224 , GRCh38.p12 chr11: 4,314,649-4,811,994 TRIM21, TRIM68, 29 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4671191copy number variation1nstd186human GRCh37 chr11: 4,229,020-4,406,520 , GRCh38.p12 chr11: 4,207,790-4,385,290 SSU72P6, OR52B4, 8 more genes
    nsv4618277copy number variation2nstd183human GRCh37 chr11: 4,229,020-4,406,520 , GRCh38.p12 chr11: 4,207,790-4,385,290 SSU72P6, SSU72L1, 8 more genes
    nsv4617849copy number variation1nstd183human GRCh37 chr11: 4,388,908-4,389,691 , GRCh38.p12 chr11: 4,367,678-4,368,461 OR52B4
    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