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 816

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968909inversion1nstd209human GRCh38 chr4: 184,990,077-186,324,974 , GRCh37.p13 chr4: 185,911,231-187,246,128 SLC25A4, F11, 25 more genes
    nsv5951635insertion1nstd209human GRCh38 chr4: 185,290,720-185,290,720 , GRCh37.p13 chr4: 186,211,874-186,211,874 SNX25
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5904270copy number variation1nstd209human GRCh38 chr4: 185,240,464-185,241,074 , GRCh37.p13 chr4: 186,161,618-186,162,228 SNX25
    nsv5899371copy number variation1nstd209human GRCh38 chr4: 185,237,868-185,239,286 , GRCh37.p13 chr4: 186,159,022-186,160,440 SNX25
    nsv5899104copy number variation1nstd209human GRCh38 chr4: 185,234,386-185,234,696 , GRCh37.p13 chr4: 186,155,540-186,155,850 SNX25
    nsv5898303copy number variation1nstd209human GRCh38 chr4: 185,210,390-185,210,441 , GRCh37.p13 chr4: 186,131,544-186,131,595 SNX25
    nsv5896919copy number variation1nstd209human GRCh38 chr4: 185,240,381-185,240,557 , GRCh37.p13 chr4: 186,161,535-186,161,711 SNX25
    nsv5891998copy number variation1nstd209human GRCh38 chr4: 185,222,031-185,222,109 , GRCh37.p13 chr4: 186,143,185-186,143,263 SNX25
    nsv5890948copy number variation1nstd209human GRCh38 chr4: 185,216,622-185,218,186 , GRCh37.p13 chr4: 186,137,776-186,139,340 SNX25
    nsv5838813copy number variation1nstd209human GRCh38 chr4: 185,216,543-185,218,142 , GRCh37.p13 chr4: 186,137,697-186,139,296 SNX25
    nsv5838752copy number variation1nstd209human GRCh38 chr4: 185,237,389-185,239,288 , GRCh37.p13 chr4: 186,158,543-186,160,442 SNX25
    nsv5838499copy number variation1nstd209human GRCh38 chr4: 185,343,908-185,345,007 , GRCh37.p13 chr4: 186,265,062-186,266,161 SNX25
    nsv5838498copy number variation1nstd209human GRCh38 chr4: 185,340,804-185,341,903 , GRCh37.p13 chr4: 186,261,958-186,263,057 SNX25
    nsv5838497copy number variation1nstd209human GRCh38 chr4: 185,318,058-185,320,166 , GRCh37.p13 chr4: 186,239,212-186,241,320 SNX25
    nsv5838496copy number variation1nstd209human GRCh38 chr4: 185,240,486-185,242,794 , GRCh37.p13 chr4: 186,161,640-186,163,948 SNX25
    nsv5838212copy number variation1nstd209human GRCh38 chr4: 185,327,196-185,328,595 , GRCh37.p13 chr4: 186,248,350-186,249,749 SNX25
    nsv5838211copy number variation1nstd209human GRCh38 chr4: 185,309,071-185,313,125 , GRCh37.p13 chr4: 186,230,225-186,234,279 SNX25
    nsv5838210copy number variation1nstd209human GRCh38 chr4: 185,287,392-185,289,127 , GRCh37.p13 chr4: 186,208,546-186,210,281 SNX25
    nsv5691811mobile element insertion2nstd211human GRCh38 chr4: 185,219,922-185,219,922 , GRCh37.p13 chr4: 186,141,076-186,141,076 SNX25
    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