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 379

    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
    nsv5949436insertion1nstd209human GRCh38 chrX: 30,868,313-30,868,313 , GRCh37.p13 chrX: 30,886,430-30,886,430 TAB3
    nsv5880006copy number variation1nstd209human GRCh38 chrX: 30,868,502-30,868,566 , GRCh37.p13 chrX: 30,886,619-30,886,683 TAB3
    nsv5876262copy number variation1nstd209human GRCh38 chrX: 30,868,311-30,868,365 , GRCh37.p13 chrX: 30,886,428-30,886,482 TAB3
    nsv5674090copy number variation1nstd102humanPathogenic GRCh37 chrX: 27,765,013-31,697,703 , GRCh38.p12 chrX: 27,746,896-31,679,586 LOC392436, MAGEB2, 32 more genes
    nsv5666926copy number variation1nstd207human GRCh38 chrX: 30,868,504-30,868,566 , GRCh37.p13 chrX: 30,886,621-30,886,683 TAB3
    nsv5424347copy number variation1nstd206human GRCh38 chrX: 30,833,118-30,833,256 , GRCh37.p13 chrX: 30,851,235-30,851,373 TAB3-AS1, TAB3
    nsv5376025translocation1nstd200human GRCh38 chrX: 30,881,258-30,881,258 , GRCh38 chrX: 30,881,315-30,881,315 , GRCh37.p13 chrX: 30,899,432-30,899,432 , GRCh37.p13 chrX: 30,899,375-30,899,375 TAB3
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4905331copy number variation1nstd200human GRCh38 chrX: 30,583,188-30,871,502 , GRCh37.p13 chrX: 30,601,305-30,889,619 FTLP2, CKS1BP6, 4 more genes
    nsv4781911copy number variation1nstd200human GRCh37 chrX: 30,843,841-30,866,300 , GRCh38.p12 chrX: 30,825,724-30,848,183 TAB3, TAB3-AS1
    nsv4781910copy number variation1nstd200human GRCh37 chrX: 30,601,305-30,889,619 , GRCh38.p12 chrX: 30,583,188-30,871,502 CKS1BP6, TAB3-AS1, 4 more genes
    nsv4779369copy number variation1nstd200human GRCh37 chrX: 28,032,402-31,547,205 , GRCh38.p12 chrX: 28,014,285-31,529,088 RNA5SP500, FTHL17, 24 more genes
    nsv4767574copy number variation1nstd199human GRCh37 chrX: 30,886,613-30,886,676 , GRCh38.p12 chrX: 30,868,496-30,868,559 TAB3
    nsv4728709copy number variation1nstd102humanUncertain significance GRCh37 chrX: 30,870,218-31,102,254 , GRCh38.p12 chrX: 30,852,101-31,084,137 FTHL17, TAB3
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4728468copy number variation1nstd102humanPathogenic GRCh37 chrX: 28,309,706-31,853,992 , GRCh38.p12 chrX: 28,291,589-31,835,875 MAGEB1, MAGEB4, 22 more genes
    nsv4682173copy number variation1nstd102humanPathogenic GRCh37 chrX: 30,326,313-41,000,684 , GRCh38.p12 chrX: 30,308,196-41,141,431 RNU6-1087P, ATP6AP2, 102 more genes
    nsv4680856copy number variation1nstd189human GRCh37.p13 chrX: 30,872,581-31,083,618 , GRCh38.p12 chrX: 30,854,464-31,065,501 TAB3
    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