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 1032

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145639insertion1nstd232human GRCh37.p13 chr5: 108,481,911-108,481,911 , GRCh38.p12 chr5: 109,146,210-109,146,210 FER
    nsv7057566inversion1nstd229human GRCh38 chr5: 108,507,567-110,438,651 , GRCh37.p13 chr5: 107,843,268-109,774,352 CT45B1P, LOC105379117, 17 more genes
    nsv7048131inversion1nstd229human GRCh38 chr5: 109,124,151-109,401,138 , GRCh37.p13 chr5: 108,459,852-108,736,839 FER, PJA2, 1 more genes
    nsv7043580inversion1nstd229human GRCh38 chr5: 108,848,269-108,855,839 , GRCh37.p13 chr5: 108,183,970-108,191,540 FER
    nsv6777968copy number variation1nstd229human GRCh38 chr5: 109,051,353-109,058,895 , GRCh37.p13 chr5: 108,387,054-108,394,596 FER, GJA1P1
    nsv6777924copy number variation1nstd229human GRCh38 chr5: 108,847,469-108,850,197 , GRCh37.p13 chr5: 108,183,170-108,185,898 FER
    nsv6777362copy number variation1nstd229human GRCh38 chr5: 109,007,016-109,007,103 , GRCh37.p13 chr5: 108,342,717-108,342,804 FER
    nsv6777174copy number variation1nstd229human GRCh38 chr5: 108,855,601-108,858,200 , GRCh37.p13 chr5: 108,191,302-108,193,901 FER
    nsv6776927copy number variation1nstd229human GRCh38 chr5: 108,904,104-108,904,138 , GRCh37.p13 chr5: 108,239,805-108,239,839 FER
    nsv6776122copy number variation1nstd229human GRCh38 chr5: 108,891,599-108,891,671 , GRCh37.p13 chr5: 108,227,300-108,227,372 FER
    nsv6775845copy number variation1nstd229human GRCh38 chr5: 108,816,307-108,830,332 , GRCh37.p13 chr5: 108,152,008-108,166,033 FER
    nsv6775111copy number variation1nstd229human GRCh38 chr5: 109,079,901-109,084,300 , GRCh37.p13 chr5: 108,415,602-108,420,001 FER
    nsv6775080copy number variation1nstd229human GRCh38 chr5: 108,983,082-108,985,703 , GRCh37.p13 chr5: 108,318,783-108,321,404 FER
    nsv6774178copy number variation1nstd229human GRCh38 chr5: 109,095,174-109,170,103 , GRCh37.p13 chr5: 108,430,875-108,505,804 FER
    nsv6773758copy number variation1nstd229human GRCh38 chr5: 109,018,001-109,074,300 , GRCh37.p13 chr5: 108,353,702-108,410,001 GJA1P1, FER
    nsv6773729copy number variation1nstd229human GRCh38 chr5: 108,799,424-108,803,801 , GRCh37.p13 chr5: 108,135,125-108,139,502 FER
    nsv6773155copy number variation1nstd229human GRCh38 chr5: 108,983,901-108,999,900 , GRCh37.p13 chr5: 108,319,602-108,335,601 FER
    nsv6772985copy number variation1nstd229human GRCh38 chr5: 109,055,553-109,068,250 , GRCh37.p13 chr5: 108,391,254-108,403,951 FER
    nsv6772930copy number variation1nstd229human GRCh38 chr5: 109,090,592-109,098,769 , GRCh37.p13 chr5: 108,426,293-108,434,470 FER
    nsv6772674copy number variation1nstd229human GRCh38 chr5: 108,740,640-108,745,765 , GRCh37.p13 chr5: 108,076,341-108,081,466 FER
    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