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 375

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137189copy number variation1nstd102humanPathogenic GRCh38 chrX: 139,530,738-139,537,009 , GRCh37.p13 chrX: 138,612,897-138,619,168 F9
    nsv7137181copy number variation1nstd102humanPathogenic GRCh37 chrX: 138,612,923-138,623,234 , GRCh38.p12 chrX: 139,530,764-139,541,075 F9
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098589copy number variation1nstd102humanUncertain significance GRCh37 chrX: 138,612,860-138,914,348 , GRCh38.p12 chrX: 139,530,701-139,832,189 BCYRN1P1, ATP11C, 2 more genes
    nsv7093564insertion1nstd102humanPathogenic GRCh37 chrX: 138,630,538-138,630,538 , GRCh38 chrX: 139,548,379-139,548,379 F9
    nsv7091159copy number variation1nstd229human GRCh38 chrX: 139,042,576-139,543,068 , GRCh37.p13 chrX: 138,124,738-138,625,227 FGF13, F9, 2 more genes
    nsv7084418copy number variation1nstd229human GRCh38 chrX: 137,855,369-139,709,654 , GRCh37.p13 chrX: 136,937,528-138,791,813 FGF13, F9, 10 more genes
    nsv7079165copy number variation1nstd229human GRCh38 chrX: 139,555,404-139,560,617 , GRCh37.p13 chrX: 138,637,563-138,642,776 F9
    nsv7079164copy number variation1nstd229human GRCh38 chrX: 139,551,196-139,583,709 , GRCh37.p13 chrX: 138,633,355-138,665,868 MCF2, F9
    nsv7079163copy number variation1nstd229human GRCh38 chrX: 139,550,857-139,552,031 , GRCh37.p13 chrX: 138,633,016-138,634,190 F9
    nsv7079162copy number variation1nstd229human GRCh38 chrX: 139,550,775-139,557,245 , GRCh37.p13 chrX: 138,632,934-138,639,404 F9
    nsv7079161copy number variation1nstd229human GRCh38 chrX: 139,549,574-139,586,742 , GRCh37.p13 chrX: 138,631,733-138,668,901 MCF2, F9
    nsv7079160copy number variation1nstd229human GRCh38 chrX: 139,544,898-139,554,912 , GRCh37.p13 chrX: 138,627,057-138,637,071 F9
    nsv7079159copy number variation1nstd229human GRCh38 chrX: 139,542,205-139,546,263 , GRCh37.p13 chrX: 138,624,364-138,628,422 F9
    nsv7079158copy number variation1nstd229human GRCh38 chrX: 139,537,399-139,632,322 , GRCh37.p13 chrX: 138,619,558-138,714,481 F9, MCF2
    nsv7079157copy number variation1nstd229human GRCh38 chrX: 139,537,231-139,614,114 , GRCh37.p13 chrX: 138,619,390-138,696,273 MCF2, F9
    nsv7079156copy number variation1nstd229human GRCh38 chrX: 139,535,449-139,800,912 , GRCh37.p13 chrX: 138,617,608-138,883,071 F9, ATP11C, 2 more genes
    nsv7079155copy number variation1nstd229human GRCh38 chrX: 139,532,440-139,694,901 , GRCh37.p13 chrX: 138,614,599-138,777,060 F9, MCF2
    nsv7079154copy number variation1nstd229human GRCh38 chrX: 139,525,901-139,853,300 , GRCh37.p13 chrX: 138,608,060-138,935,459 MCF2, F9, 2 more genes
    nsv7079153copy number variation1nstd229human GRCh38 chrX: 139,525,855-139,852,250 , GRCh37.p13 chrX: 138,608,014-138,934,409 ATP11C, MCF2, 2 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