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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148259copy number variation1nstd102humanPathogenic GRCh38 chrX: 150,592,508-150,619,237 , GRCh37.p13 chrX|NW_004070890.2: 6,116,906-6,143,635 , GRCh37.p13 chrX: 149,760,970-149,787,710 MTM1
    nsv7137088copy number variation1nstd102humanPathogenic GRCh37 chrX: 149,761,077-149,818,374 , GRCh38.p12 chrX: 150,592,615-150,649,901 MTM1
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098996copy number variation1nstd102humanPathogenic GRCh38 chrX: 150,568,597-150,568,662 , GRCh37 chrX: 149,737,047-149,737,112 MTM1
    nsv7098869copy number variation1nstd102humanPathogenic GRCh37 chrX: 139,586,015-154,774,957 , GRCh38.p12 chrX: 140,503,850-155,545,296 MAGEA6, LOC101928832, 303 more genes
    nsv7098594copy number variation1nstd102humanUncertain significance GRCh37 chrX: 149,761,077-149,787,632 , GRCh38.p12 chrX: 150,592,615-150,619,159 MTM1
    nsv7098348copy number variation1nstd102humanUncertain significance GRCh37 chrX: 149,613,783-149,840,068 , GRCh38.p12 chrX: 150,445,517-150,671,595 MTM1, MAMLD1
    nsv7098232copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 149,613,783-150,573,536 , GRCh38.p12 chrX: 150,445,517-151,405,064 MTM1, GPR50, 14 more genes
    nsv7097994copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 149,818,176-149,818,384 , GRCh38.p12 chrX: 150,649,703-150,649,911 MTM1
    nsv7097993copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 149,761,093-149,767,213 , GRCh38.p12 chrX: 150,592,631-150,598,749 MTM1
    nsv7091187copy number variation1nstd229human GRCh38 chrX: 150,668,453-150,668,631 , GRCh37.p13 chrX|NW_004070890.2: 6,192,851-6,193,029 , GRCh37.p13 chrX: 149,836,926-149,837,104 MTM1
    nsv7091186copy number variation1nstd229human GRCh38 chrX: 150,660,745-150,784,711 , GRCh37.p13 chrX|NW_004070890.2: 6,185,143-6,309,109 , GRCh37.p13 chrX: 149,829,218-149,953,184 CYP2C64P, CD99L2, 2 more genes
    nsv7091185copy number variation1nstd229human GRCh38 chrX: 150,632,767-150,632,902 , GRCh37.p13 chrX: 149,801,240-149,801,375 , GRCh37.p13 chrX|NW_004070890.2: 6,157,165-6,157,300 MTM1
    nsv7091184copy number variation1nstd229human GRCh38 chrX: 150,589,501-150,591,400 , GRCh37.p13 chrX|NW_004070890.2: 6,113,899-6,115,798 , GRCh37.p13 chrX: 149,757,963-149,759,862 MTM1
    nsv7091183copy number variation1nstd229human GRCh38 chrX: 150,578,002-150,578,289 , GRCh37.p13 chrX|NW_004070890.2: 6,102,400-6,102,687 , GRCh37.p13 chrX: 149,746,458-149,746,745 MTM1
    nsv7091171copy number variation1nstd229human GRCh38 chrX: 150,262,588-151,080,792 , GRCh37.p13 chrX: 149,430,802-150,174,083 , GRCh37.p13 chrX|NW_004070890.2: 5,786,986-6,530,008 RNA5SP525, CD99L2, 9 more genes
    nsv7091170copy number variation1nstd229human GRCh38 chrX: 150,253,215-151,011,085 , GRCh37.p13 chrX|NW_004070890.2: 5,777,613-6,530,008 , GRCh37.p13 chrX: 149,421,426-150,174,083 CYP2C64P, MAMLD1, 7 more genes
    nsv7085435copy number variation1nstd229human GRCh38 chrX: 150,227,830-151,085,680 , GRCh37.p13 chrX|NW_004070890.2: 5,752,228-6,530,008 , GRCh37.p13 chrX: 149,396,065-150,174,083 XRCC6P2, RNU6-383P, 11 more genes
    nsv7085422copy number variation1nstd229human GRCh38 chrX: 150,135,119-150,908,837 , GRCh37.p13 chrX|NW_004070890.2: 5,659,517-6,433,235 , GRCh37.p13 chrX: 149,303,349-150,077,310 MTMR1, CD99L2, 6 more genes
    nsv7055224inversion1nstd229human GRCh38 chrX: 149,372,897-150,622,533 , GRCh37.p13 chrX: 148,454,427-149,791,006 , GRCh37.p13 chrX|NW_004070890.2: 4,897,294-6,146,931 HSFX1, LOC100420322, 28 more genes
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