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 941

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142510insertion1nstd232human GRCh37.p13 chr2: 153,485,047-153,485,047 , GRCh38.p12 chr2: 152,628,533-152,628,533 FMNL2
    nsv7141742copy number variation1nstd232human GRCh37.p13 chr2: 153,399,129-153,399,179 , GRCh38.p12 chr2: 152,542,615-152,542,665 FMNL2
    nsv7141092insertion1nstd232human GRCh37.p13 chr2: 153,248,280-153,248,280 , GRCh38.p12 chr2: 152,391,766-152,391,766 FMNL2
    nsv7047013inversion1nstd229human GRCh38 chr2: 152,603,405-152,604,921 , GRCh37.p13 chr2: 153,459,919-153,461,435 FMNL2
    nsv7044640inversion1nstd229human GRCh38 chr2: 152,552,677-152,552,703 , GRCh37.p13 chr2: 153,409,191-153,409,217 FMNL2
    nsv7039838inversion1nstd229human GRCh38 chr2: 152,604,582-152,604,933 , GRCh37.p13 chr2: 153,461,096-153,461,447 FMNL2
    nsv7039180inversion1nstd229human GRCh38 chr2: 152,587,291-152,590,988 , GRCh37.p13 chr2: 153,443,805-153,447,502 FMNL2
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6698051copy number variation1nstd229human GRCh38 chr2: 152,371,873-152,484,578 , GRCh37.p13 chr2: 153,228,387-153,341,092 NUDCP1, FMNL2
    nsv6696919copy number variation1nstd229human GRCh38 chr2: 152,502,727-152,505,206 , GRCh37.p13 chr2: 153,359,241-153,361,720 FMNL2
    nsv6695831copy number variation1nstd229human GRCh38 chr2: 152,485,559-152,500,614 , GRCh37.p13 chr2: 153,342,073-153,357,128 FMNL2
    nsv6695808copy number variation1nstd229human GRCh38 chr2: 152,423,234-152,423,453 , GRCh37.p13 chr2: 153,279,748-153,279,967 FMNL2
    nsv6695633copy number variation1nstd229human GRCh38 chr2: 152,471,173-152,472,461 , GRCh37.p13 chr2: 153,327,687-153,328,975 FMNL2
    nsv6693399copy number variation1nstd229human GRCh38 chr2: 152,590,982-152,596,183 , GRCh37.p13 chr2: 153,447,496-153,452,697 FMNL2
    nsv6693293copy number variation1nstd229human GRCh38 chr2: 152,401,414-152,405,536 , GRCh37.p13 chr2: 153,257,928-153,262,050 FMNL2
    nsv6693155copy number variation1nstd229human GRCh38 chr2: 152,619,201-152,682,300 , GRCh37.p13 chr2: 153,475,715-153,538,814 PRPF40A, FMNL2
    nsv6692771copy number variation1nstd229human GRCh38 chr2: 152,443,577-152,447,359 , GRCh37.p13 chr2: 153,300,091-153,303,873 FMNL2
    nsv6692708copy number variation1nstd229human GRCh38 chr2: 152,368,257-152,388,218 , GRCh37.p13 chr2: 153,224,771-153,244,732 NUDCP1, FMNL2
    nsv6692524copy number variation1nstd229human GRCh38 chr2: 150,229,231-153,083,013 , GRCh37.p13 chr2: 151,085,745-153,939,527 RPL30P2, NEB, 30 more genes
    nsv6690862copy number variation1nstd229human GRCh38 chr2: 152,476,690-152,484,761 , GRCh37.p13 chr2: 153,333,204-153,341,275 FMNL2
    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