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
    nsv6115990copy number variation1nstd186human GRCh37 chrX: 138,146,436-138,146,696 , GRCh38.p12 chrX: 139,064,274-139,064,534 FGF13
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5975806copy number variation1nstd209human GRCh38 chrX: 138,837,640-138,842,339 , GRCh37.p13 chrX: 137,919,802-137,924,501 FGF13
    nsv5968506copy number variation1nstd209human GRCh38 chrX: 139,039,940-139,049,453 , GRCh37.p13 chrX: 138,122,102-138,131,615 FGF13
    nsv5950449insertion1nstd209human GRCh38 chrX: 138,978,266-138,978,266 , GRCh37.p13 chrX: 138,060,428-138,060,428 FGF13
    nsv5883611copy number variation1nstd209human GRCh38 chrX: 138,838,127-138,842,209 , GRCh37.p13 chrX: 137,920,289-137,924,371 FGF13
    nsv5881120copy number variation1nstd209human GRCh38 chrX: 139,152,313-139,152,374 , GRCh37.p13 chrX: 138,234,475-138,234,536 FGF13
    nsv5881101copy number variation1nstd209human GRCh38 chrX: 138,908,028-138,908,142 , GRCh37.p13 chrX: 137,990,190-137,990,304 FGF13
    nsv5880295copy number variation1nstd209human GRCh38 chrX: 139,040,423-139,048,567 , GRCh37.p13 chrX: 138,122,585-138,130,729 FGF13
    nsv5878022copy number variation1nstd209human GRCh38 chrX: 139,070,008-139,074,249 , GRCh37.p13 chrX: 138,152,170-138,156,411 FGF13
    nsv5877768copy number variation1nstd209human GRCh38 chrX: 139,144,334-139,144,489 , GRCh37.p13 chrX: 138,226,496-138,226,651 FGF13
    nsv5874260copy number variation1nstd209human GRCh38 chrX: 138,999,681-139,000,308 , GRCh37.p13 chrX: 138,081,843-138,082,470 FGF13
    nsv5870056copy number variation1nstd209human GRCh38 chrX: 139,064,256-139,064,533 , GRCh37.p13 chrX: 138,146,418-138,146,695 FGF13
    nsv5869407copy number variation1nstd209human GRCh38 chrX: 138,625,467-138,625,536 , GRCh37.p13 chrX: 137,707,628-137,707,697 FGF13
    nsv5868974copy number variation1nstd209human GRCh38 chrX: 139,075,824-139,076,013 , GRCh37.p13 chrX: 138,157,986-138,158,175 FGF13
    nsv5729823mobile element insertion1nstd211human GRCh38 chrX: 138,998,411-138,998,411 , GRCh37.p13 chrX: 138,080,573-138,080,573 FGF13
    nsv5729788mobile element insertion2nstd211human GRCh38 chrX: 139,158,999-139,158,999 , GRCh37.p13 chrX: 138,241,161-138,241,161 FGF13
    nsv5729068mobile element insertion1nstd211human GRCh38 chrX: 139,136,266-139,136,266 , GRCh37.p13 chrX: 138,218,428-138,218,428 FGF13
    nsv5728742mobile element insertion1nstd211human GRCh38 chrX: 139,181,439-139,181,439 , GRCh37.p13 chrX: 138,263,601-138,263,601 FGF13
    nsv5727695mobile element insertion1nstd211human GRCh38 chrX: 139,164,688-139,164,688 , GRCh37.p13 chrX: 138,246,850-138,246,850 FGF13
    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