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 451

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 more genes
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098323copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,222,149-55,057,617 , GRCh38.p12 chrX: 53,192,967-55,031,184 RPL37P24, KDM5C, 34 more genes
    nsv7091928copy number variation1nstd229human GRCh38 chrX: 54,029,380-54,032,445 , GRCh37.p13 chrX: 54,055,813-54,058,878 , GRCh37.p13 chrX|NW_004070877.1: 3,742,495-3,745,560 PHF8
    nsv7091927copy number variation1nstd229human GRCh38 chrX: 53,998,201-54,164,200 , GRCh37.p13 chrX|NW_004070877.1: 3,711,316-3,877,315 , GRCh37.p13 chrX: 54,024,634-54,190,633 RPL37P24, FAM120C, 1 more genes
    nsv7091926copy number variation1nstd229human GRCh38 chrX: 53,976,216-53,978,710 , GRCh37.p13 chrX: 54,002,649-54,005,143 , GRCh37.p13 chrX|NW_004070877.1: 3,689,331-3,691,825 PHF8
    nsv7091925copy number variation1nstd229human GRCh38 chrX: 53,969,582-53,971,887 , GRCh37.p13 chrX: 53,996,015-53,998,320 , GRCh37.p13 chrX|NW_004070877.1: 3,682,697-3,685,002 PHF8
    nsv7091924copy number variation1nstd229human GRCh38 chrX: 53,959,601-54,145,500 , GRCh37.p13 chrX|NW_004070877.1: 3,672,716-3,858,615 , GRCh37.p13 chrX: 53,986,034-54,171,933 FAM120C, RPL37P24, 1 more genes
    nsv7091915copy number variation1nstd229human GRCh38 chrX: 53,846,924-54,010,321 , GRCh37.p13 chrX|NW_004070877.1: 3,560,039-3,723,436 , GRCh37.p13 chrX: 53,873,350-54,036,754 PHF8, RNA5SP505
    nsv7091907copy number variation1nstd229human GRCh38 chrX: 53,781,353-53,942,863 , GRCh37.p13 chrX|NW_004070877.1: 3,494,468-3,655,978 , GRCh37.p13 chrX: 53,807,851-53,969,296 MRPS18CP7, RNA5SP505, 1 more genes
    nsv7091904copy number variation1nstd229human GRCh38 chrX: 53,763,602-53,993,288 , GRCh37.p13 chrX: 53,790,100-54,019,721 , GRCh37.p13 chrX|NW_004070877.1: 3,476,717-3,706,403 PHF8, RNA5SP505, 1 more genes
    nsv7091897copy number variation1nstd229human GRCh38 chrX: 53,716,401-53,945,300 , GRCh37.p13 chrX|NW_004070877.1: 3,429,516-3,658,415 , GRCh37.p13 chrX: 53,743,344-53,971,733 RNA5SP505, MRPS18CP7, 1 more genes
    nsv7091893copy number variation1nstd229human GRCh38 chrX: 53,686,201-53,951,900 , GRCh37.p13 chrX: 53,713,146-53,978,333 , GRCh37.p13 chrX|NW_004070877.1: 3,399,316-3,665,015 MRPS18CP7, PHF8, 2 more genes
    nsv7091890copy number variation1nstd229human GRCh38 chrX: 53,662,985-53,945,531 , GRCh37.p13 chrX|NW_004070877.1: 3,376,100-3,658,646 , GRCh37.p13 chrX: 53,689,939-53,971,964 HUWE1, RNA5SP505, 2 more genes
    nsv7030885inversion1nstd229human GRCh38 chrX: 52,934,179-55,490,651 , GRCh37.p13 chrX|NW_004070877.1: 2,647,294-4,110,759 , GRCh37.p13 chrX: 52,963,388-54,424,077 MRPS18CP7, TRO, 58 more genes
    nsv7030255inversion1nstd229human GRCh38 chrX: 53,559,743-53,945,305 , GRCh37.p13 chrX: 53,586,704-53,971,738 , GRCh37.p13 chrX|NW_004070877.1: 3,272,858-3,658,420 MRPS18CP7, RNA5SP505, 2 more genes
    nsv7025237inversion1nstd229human GRCh38 chrX: 50,557,525-57,228,328 , GRCh37.p13 chrX|NW_004070877.1: 270,640-4,110,759 , GRCh37.p13 chrX: 50,300,525-54,424,077 UBQLN2, IPO7P1, 141 more genes
    nsv7021646inversion1nstd229human GRCh38 chrX: 53,718,349-55,635,499 , GRCh37.p13 chrX: 54,424,078-55,661,932 RNA5SP505, MIR4536-2, 40 more genes
    nsv6636847copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,922,255-54,064,919 , GRCh38.p12 chrX: 53,895,836-54,038,486 PHF8, RNA5SP505
    nsv6636598copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,911,258-54,049,774 , GRCh38.p12 chrX: 53,884,839-54,023,341 PHF8, RNA5SP505
    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