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 489

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7054725inversion1nstd229human GRCh38 chr4: 178,850,585-188,333,056 , GRCh37.p13 chr4: 179,771,739-189,254,210 RPL6P16, LOC105377568, 125 more genes
    nsv7054658inversion1nstd229human GRCh38 chr4: 183,954,061-185,864,650 , GRCh37.p13 chr4: 184,875,214-186,785,804 IRF2, LOC105377590, 39 more genes
    nsv7051710inversion1nstd229human GRCh38 chr4: 184,496,747-186,979,683 , GRCh37.p13 chr4: 185,417,901-187,900,837 LOC102723906, LINC02436, 47 more genes
    nsv7051528inversion1nstd229human GRCh38 chr4: 185,166,451-185,246,476 , GRCh37.p13 chr4: 186,087,605-186,167,630 SNX25, CFAP97
    nsv7049975inversion1nstd229human GRCh38 chr4: 185,170,243-185,292,629 , GRCh37.p13 chr4: 186,091,397-186,213,783 SNX25, CFAP97
    nsv7049486inversion1nstd229human GRCh38 chr4: 185,167,721-185,167,802 , GRCh37.p13 chr4: 186,088,875-186,088,956 CFAP97
    nsv7048281inversion1nstd229human GRCh38 chr4: 177,590,230-186,282,308 , GRCh37.p13 chr4: 178,511,384-187,203,462 STOX2, LINC01098, 105 more genes
    nsv7045756inversion1nstd229human GRCh38 chr4: 185,161,194-185,161,435 , GRCh37.p13 chr4: 186,082,348-186,082,589 CFAP97
    nsv7045478inversion1nstd229human GRCh38 chr4: 184,811,410-187,241,218 , GRCh37.p13 chr4: 185,732,564-188,162,372 RPSAP70, MIR3945, 42 more genes
    nsv7044886inversion1nstd229human GRCh38 chr4: 185,127,051-188,186,487 , GRCh37.p13 chr4: 186,048,205-189,107,641 SORBS2, F11-AS1, 50 more genes
    nsv7043815inversion1nstd229human GRCh38 chr4: 185,197,677-185,198,556 , GRCh37.p13 chr4: 186,118,831-186,119,710 CFAP97
    nsv7041154inversion1nstd229human GRCh38 chr4: 184,990,240-187,505,802 , GRCh37.p13 chr4: 185,911,394-188,426,956 F11-AS1, MTNR1A, 40 more genes
    nsv7038937inversion1nstd229human GRCh38 chr4: 185,006,974-188,807,470 , GRCh37.p13 chr4: 185,928,128-189,728,624 LOC105377609, FAUP3, 63 more genes
    nsv6757431copy number variation1nstd229human GRCh38 chr4: 185,181,201-185,238,300 , GRCh37.p13 chr4: 186,102,355-186,159,454 SNX25, CFAP97
    nsv6757036copy number variation1nstd229human GRCh38 chr4: 185,163,273-185,166,537 , GRCh37.p13 chr4: 186,084,427-186,087,691 CFAP97
    nsv6756944copy number variation1nstd229human GRCh38 chr4: 184,402,149-185,513,891 , GRCh37.p13 chr4: 185,323,303-186,435,045 LINC02365, SNX25, 27 more genes
    nsv6755147copy number variation1nstd229human GRCh38 chr4: 184,958,301-185,210,600 , GRCh37.p13 chr4: 185,879,455-186,131,754 SNX25, CFAP97, 5 more genes
    nsv6754462copy number variation1nstd229human GRCh38 chr4: 185,162,528-185,167,266 , GRCh37.p13 chr4: 186,083,682-186,088,420 CFAP97
    nsv6754396copy number variation1nstd229human GRCh38 chr4: 185,178,953-185,180,619 , GRCh37.p13 chr4: 186,100,107-186,101,773 CFAP97
    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