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 338

    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
    nsv5872026copy number variation1nstd209human GRCh38 chrX: 81,283,765-81,283,922 , GRCh37.p13 chrX: 80,539,264-80,539,421 SH3BGRL
    nsv5723264mobile element insertion1nstd211human GRCh38 chrX: 81,213,627-81,213,627 , GRCh37.p13 chrX: 80,469,126-80,469,126 SH3BGRL
    nsv5714844mobile element insertion2nstd211human GRCh38 chrX: 81,222,557-81,222,557 , GRCh37.p13 chrX: 80,478,056-80,478,056 SH3BGRL
    nsv5563883mobile element insertion1nstd206human GRCh38 chrX: 81,222,557-81,222,608 , GRCh37.p13 chrX: 80,478,056-80,478,107 SH3BGRL
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5433593copy number variation1nstd206human GRCh38 chrX: 81,285,991-81,288,027 , GRCh37.p13 chrX: 80,541,490-80,543,526 SH3BGRL
    nsv5417362copy number variation1nstd206human GRCh38 chrX: 81,207,568-81,208,521 , GRCh37.p13 chrX: 80,463,067-80,464,020 SH3BGRL
    nsv5376576translocation1nstd200human GRCh38 chrX: 81,283,768-81,283,768 , GRCh38 chrX: 81,283,923-81,283,923 , GRCh37.p13 chrX: 80,539,422-80,539,422 , GRCh37.p13 chrX: 80,539,267-80,539,267 SH3BGRL
    nsv5196573mobile element insertion1nstd203human GRCh38 chrX: 81,213,612-81,213,627 , GRCh37.p13 chrX: 80,469,111-80,469,126 SH3BGRL
    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
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4771628copy number variation1nstd200human GRCh37 chrX: 80,541,490-80,543,526 , GRCh38.p12 chrX: 81,285,991-81,288,027 SH3BGRL
    nsv4771627copy number variation1nstd200human GRCh37 chrX: 80,484,456-80,485,083 , GRCh38.p12 chrX: 81,228,957-81,229,584 SH3BGRL
    nsv4769249copy number variation1nstd201human GRCh37 chrX: 61,728,816-155,233,846 , GRCh38.p12 chrX: 62,509,346-156,004,181 , ABCB7, 1364 more genes
    nsv4728601copy number variation1nstd102humanPathogenic GRCh37 chrX: 77,514,079-127,770,854 , GRCh38.p12 chrX: 78,258,582-128,636,876 PHB1P10, SNORA35, 565 more genes
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4674753copy number variation1nstd102humanPathogenic GRCh37 chrX: 78,444,738-155,233,731 , GRCh38.p12 chrX: 79,189,241-156,004,066 PAK3, ZCCHC12, 1069 more genes
    nsv4663739copy number variation1nstd186human GRCh37 chrX: 80,463,067-80,464,020 , GRCh38.p12 chrX: 81,207,568-81,208,521 SH3BGRL
    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