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 354

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5876669copy number variation1nstd209human GRCh38 chrX: 136,727,426-136,727,543 , GRCh37.p13 chrX: 135,809,585-135,809,702 ARHGEF6
    nsv5730953mobile element insertion1nstd211human GRCh38 chrX: 136,745,763-136,745,763 , GRCh37.p13 chrX: 135,827,922-135,827,922 ARHGEF6
    nsv5715867mobile element insertion1nstd211human GRCh38 chrX: 136,687,410-136,687,410 , GRCh37.p13 chrX: 135,769,569-135,769,569 ARHGEF6
    nsv5560085mobile element insertion1nstd206human GRCh38 chrX: 136,687,410-136,687,420 , GRCh37.p13 chrX: 135,769,569-135,769,579 ARHGEF6
    nsv5555853mobile element insertion1nstd206human GRCh38 chrX: 136,745,763-136,745,814 , GRCh37.p13 chrX: 135,827,922-135,827,973 ARHGEF6
    nsv5377122translocation1nstd200human GRCh38 chrX: 136,753,467-136,753,467 , GRCh38 chrX: 136,747,391-136,747,391 , GRCh37.p13 chrX: 135,829,550-135,829,550 , GRCh37.p13 chrX: 135,835,626-135,835,626 ARHGEF6
    nsv5331881translocation1nstd200human GRCh37 chrX: 135,809,093-135,809,093 , GRCh37 chrX: 135,808,991-135,808,991 , GRCh38.p12 chrX: 136,726,934-136,726,934 , GRCh38.p12 chrX: 136,726,832-136,726,832 ARHGEF6
    nsv5187340mobile element insertion1nstd203human GRCh38 chrX: 136,731,280-136,731,290 , GRCh37.p13 chrX: 135,813,439-135,813,449 ARHGEF6
    nsv5185719mobile element insertion1nstd203human GRCh38 chrX: 136,758,373-136,758,388 , GRCh37.p13 chrX: 135,840,532-135,840,547 ARHGEF6
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5041083inversion1nstd200human GRCh38 chrX: 136,450,318-138,402,964 , GRCh37.p13 chrX: 135,532,477-137,485,123 SRRM1P3, TM9SF5P, 23 more genes
    nsv4909174copy number variation1nstd200human GRCh38 chrX: 136,769,595-136,769,770 , GRCh37.p13 chrX: 135,851,754-135,851,929 ARHGEF6
    nsv4909173copy number variation1nstd200human GRCh38 chrX: 136,755,533-136,755,721 , GRCh37.p13 chrX: 135,837,692-135,837,880 ARHGEF6
    nsv4909172copy number variation1nstd200human GRCh38 chrX: 136,643,422-137,209,295 , GRCh37.p13 chrX: 135,725,581-136,291,454 SNORD61, CD40LG, 11 more genes
    nsv4872387inversion1nstd200human GRCh37 chrX: 135,532,477-137,485,129 , GRCh38.p12 chrX: 136,450,318-138,402,970 SNORD61, CD40LG, 23 more genes
    nsv4782364copy number variation1nstd200human GRCh37 chrX: 135,851,754-135,851,929 , GRCh38.p12 chrX: 136,769,595-136,769,770 ARHGEF6
    nsv4769250copy number variation1nstd201human GRCh37 chrX: 96,096,220-155,208,244 , GRCh38.p12 chrX: 96,841,221-155,978,579 , AGTR2, 959 more genes
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728533copy number variation1nstd102humanPathogenic GRCh37 chrX: 94,264,404-155,233,731 , GRCh38.p12 chrX: 95,009,405-156,004,066 CT45A10, MIR224, 968 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