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 456

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056794inversion1nstd229human GRCh38 chr2: 36,938,664-36,944,722 , GRCh37.p13 chr2: 37,165,807-37,171,865 STRN
    nsv6677614copy number variation1nstd229human GRCh38 chr2: 36,957,201-37,052,100 , GRCh37.p13 chr2: 37,184,344-37,279,243 STRN, HEATR5B
    nsv6673916copy number variation1nstd229human GRCh38 chr2: 36,912,151-36,912,343 , GRCh37.p13 chr2: 37,139,294-37,139,486 STRN
    nsv6669741copy number variation1nstd229human GRCh38 chr2: 36,963,240-36,965,100 , GRCh37.p13 chr2: 37,190,383-37,192,243 STRN
    nsv6668608copy number variation1nstd229human GRCh38 chr2: 36,947,391-36,948,619 , GRCh37.p13 chr2: 37,174,534-37,175,762 STRN
    nsv6667868copy number variation1nstd229human GRCh38 chr2: 36,795,926-36,837,923 , GRCh37.p13 chr2: 37,023,069-37,065,066 STRN, VIT
    nsv6665375copy number variation1nstd229human GRCh38 chr2: 36,801,678-36,869,460 , GRCh37.p13 chr2: 37,028,821-37,096,603 VIT, STRN, 1 more genes
    nsv6664015copy number variation1nstd229human GRCh38 chr2: 36,854,429-36,855,584 , GRCh37.p13 chr2: 37,081,572-37,082,727 STRN
    nsv6663603copy number variation1nstd229human GRCh38 chr2: 36,919,863-36,919,977 , GRCh37.p13 chr2: 37,147,006-37,147,120 STRN
    nsv6662875copy number variation1nstd229human GRCh38 chr2: 36,893,404-37,048,540 , GRCh37.p13 chr2: 37,120,547-37,275,683 STRN, HEATR5B
    nsv6662814copy number variation1nstd229human GRCh38 chr2: 36,935,884-36,945,644 , GRCh37.p13 chr2: 37,163,027-37,172,787 STRN
    nsv6662608copy number variation1nstd229human GRCh38 chr2: 36,897,517-36,897,601 , GRCh37.p13 chr2: 37,124,660-37,124,744 STRN
    nsv6659170copy number variation1nstd229human GRCh38 chr2: 36,945,076-36,946,772 , GRCh37.p13 chr2: 37,172,219-37,173,915 STRN
    nsv6658991copy number variation1nstd229human GRCh38 chr2: 36,946,152-36,946,223 , GRCh37.p13 chr2: 37,173,295-37,173,366 STRN
    nsv6658479copy number variation1nstd229human GRCh38 chr2: 36,949,551-36,964,183 , GRCh37.p13 chr2: 37,176,694-37,191,326 STRN
    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
    nsv6551896inversion1nstd223human GRCh38 chr2: 36,941,133-36,941,601 , GRCh37.p13 chr2: 37,168,276-37,168,744 STRN
    nsv6551243inversion1nstd223human GRCh38 chr2: 36,953,969-36,954,684 , GRCh37.p13 chr2: 37,181,112-37,181,827 STRN
    nsv6549542inversion1nstd223human GRCh38 chr2: 32,866,974-37,651,961 , GRCh37.p13 chr2: 33,092,041-37,879,104 QPCT, TYW1P1, 55 more genes
    nsv6548859inversion1nstd223human GRCh38 chr2: 32,866,975-38,526,880 , GRCh37.p13 chr2: 33,092,042-38,754,022 ATP6V0E1P3, ARL14EPP1, 76 more genes
    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