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 248

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6674310copy number variation1nstd229human GRCh38 chr2: 64,930,540-64,933,883 , GRCh37.p13 chr2: 65,157,674-65,161,017 LINC02245
    nsv6674094copy number variation1nstd229human GRCh38 chr2: 64,917,541-64,926,652 , GRCh37.p13 chr2: 65,144,675-65,153,786 LINC02245
    nsv6672326copy number variation1nstd229human GRCh38 chr2: 64,902,304-64,912,321 , GRCh37.p13 chr2: 65,129,438-65,139,455 RN7SL211P, LINC02245
    nsv6671228copy number variation1nstd229human GRCh38 chr2: 64,912,602-64,913,363 , GRCh37.p13 chr2: 65,139,736-65,140,497 LINC02245
    nsv6670871copy number variation1nstd229human GRCh38 chr2: 64,891,390-64,922,013 , GRCh37.p13 chr2: 65,118,524-65,149,147 LINC02245, RN7SL211P
    nsv6668265copy number variation1nstd229human GRCh38 chr2: 64,928,562-64,937,342 , GRCh37.p13 chr2: 65,155,696-65,164,476 LINC02245
    nsv6666860copy number variation1nstd229human GRCh38 chr2: 64,903,451-64,904,118 , GRCh37.p13 chr2: 65,130,585-65,131,252 LINC02245
    nsv6665246copy number variation1nstd229human GRCh38 chr2: 64,902,305-64,907,782 , GRCh37.p13 chr2: 65,129,439-65,134,916 RN7SL211P, LINC02245
    nsv6664601copy number variation1nstd229human GRCh38 chr2: 64,921,420-64,925,425 , GRCh37.p13 chr2: 65,148,554-65,152,559 LINC02245
    nsv6661490copy number variation1nstd229human GRCh38 chr2: 64,210,609-64,960,847 , GRCh37.p13 chr2: 64,437,743-65,187,981 RN7SL211P, RNU6-100P, 23 more genes
    nsv6637048copy number variation1nstd102humanUncertain significance GRCh37 chr2: 65,110,275-65,556,249 , GRCh38.p12 chr2: 64,883,141-65,329,115 CEP68, SLC1A4, 9 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6553456inversion1nstd223human GRCh38 chr2: 64,924,875-64,926,730 , GRCh37.p13 chr2: 65,152,009-65,153,864 LINC02245
    nsv6553039inversion1nstd223human GRCh38 chr2: 64,909,181-64,909,873 , GRCh37.p13 chr2: 65,136,315-65,137,007 LINC02245
    nsv6551094inversion1nstd223human GRCh38 chr2: 64,078,330-67,334,177 , GRCh37.p13 chr2: 64,305,464-67,561,309 LINC01805, LINC02579, 59 more genes
    nsv6546524inversion1nstd223human GRCh38 chr2: 64,900,172-64,900,713 , GRCh37.p13 chr2: 65,127,306-65,127,847 LINC02245
    nsv6342257copy number variation1nstd223human GRCh38 chr2: 64,917,601-64,926,600 , GRCh37.p13 chr2: 65,144,735-65,153,734 LINC02245
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6295244copy number variation1nstd186human GRCh37 chr2: 65,139,502-65,141,199 , GRCh38.p12 chr2: 64,912,368-64,914,065 LINC02245
    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