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 2577

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963353insertion1nstd209human GRCh38 chr8: 32,366,874-32,366,874 , GRCh37.p13 chr8: 32,224,390-32,224,390 NRG1
    nsv5963182insertion1nstd209human GRCh38 chr8: 32,502,455-32,502,455 , GRCh37.p13 chr8: 32,359,971-32,359,971 NRG1
    nsv5962714insertion1nstd209human GRCh38 chr8: 32,040,750-32,040,750 , GRCh37.p13 chr8: 31,898,266-31,898,266 NRG1, NRG1-IT1
    nsv5958867insertion1nstd209human GRCh38 chr8: 31,925,168-31,925,168 , GRCh37.p13 chr8: 31,782,684-31,782,684 NRG1
    nsv5958697insertion1nstd209human GRCh38 chr8: 31,813,516-31,813,516 , GRCh37.p13 chr8: 31,671,032-31,671,032 NRG1
    nsv5954116insertion1nstd209human GRCh38 chr8: 32,634,099-32,634,099 , GRCh37.p13 chr8: 32,491,617-32,491,617 NRG1
    nsv5953445insertion1nstd209human GRCh38 chr8: 32,044,913-32,044,913 , GRCh37.p13 chr8: 31,902,429-31,902,429 NRG1, NRG1-IT1
    nsv5950457insertion1nstd209human GRCh38 chr8: 32,412,453-32,412,453 , GRCh37.p13 chr8: 32,269,969-32,269,969 NRG1
    nsv5949961insertion1nstd209human GRCh38 chr8: 32,514,936-32,514,936 , GRCh37.p13 chr8: 32,372,452-32,372,452 NRG1
    nsv5927442copy number variation1nstd209human GRCh38 chr8: 31,956,143-31,960,831 , GRCh37.p13 chr8: 31,813,659-31,818,347 NRG1
    nsv5927016copy number variation1nstd209human GRCh38 chr8: 32,204,127-32,214,796 , GRCh37.p13 chr8: 32,061,643-32,072,312 NRG1
    nsv5925205copy number variation1nstd209human GRCh38 chr8: 31,823,363-31,823,434 , GRCh37.p13 chr8: 31,680,879-31,680,950 NRG1
    nsv5923265copy number variation1nstd209human GRCh38 chr8: 32,294,713-32,297,475 , GRCh37.p13 chr8: 32,152,229-32,154,991 NRG1
    nsv5922398copy number variation1nstd209human GRCh38 chr8: 31,999,731-32,004,161 , GRCh37.p13 chr8: 31,857,247-31,861,677 NRG1
    nsv5921474copy number variation1nstd209human GRCh38 chr8: 32,604,195-32,604,244 , GRCh37.p13 chr8: 32,461,713-32,461,762 NRG1
    nsv5918376copy number variation1nstd209human GRCh38 chr8: 31,960,867-31,967,605 , GRCh37.p13 chr8: 31,818,383-31,825,121 NRG1
    nsv5918238copy number variation1nstd209human GRCh38 chr8: 31,956,050-31,967,449 , GRCh37.p13 chr8: 31,813,566-31,824,965 NRG1
    nsv5918019copy number variation1nstd209human GRCh38 chr8: 32,134,940-32,367,244 , GRCh37.p13 chr8: 31,992,456-32,224,760 NRG1, RNA5SP263, 2 more genes
    nsv5917367copy number variation1nstd209human GRCh38 chr8: 32,162,606-32,162,804 , GRCh37.p13 chr8: 32,020,122-32,020,320 NRG1
    nsv5916891copy number variation1nstd209human GRCh38 chr8: 31,713,725-31,714,077 , GRCh37.p13 chr8: 31,571,241-31,571,593 NRG1
    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