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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    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
    nsv7098604copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,490,088-154,563,736 , GRCh38.p12 chrX: 155,260,803-155,334,427 PHF10P1, CLIC2, 2 more genes
    nsv7098599copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,001,546-154,563,736 , GRCh38.p12 chrX: 153,736,092-155,334,427 TAFAZZIN, LOC105373386, 82 more genes
    nsv7097996copy number variation6nstd102humanPathogenic GRCh37 chrX: 152,014,869-155,171,615 , GRCh38.p12 chrX: 152,846,325-155,941,951 PHF10P1, ZNF185, 132 more genes
    nsv7097995copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 152,014,869-154,563,736 , GRCh38.p12 chrX: 152,846,325-155,334,427 RN7SL697P, CYCSP45, 118 more genes
    nsv7085618copy number variation1nstd229human GRCh38 chrX: 155,285,776-155,289,324 , GRCh37.p13 chrX|NW_003871103.3: 2,719,755-2,723,303 , GRCh37.p13 chrX: 154,515,067-154,518,615 CLIC2, TWF1P2
    nsv7085598copy number variation1nstd229human GRCh38 chrX: 155,180,740-155,650,140 , GRCh37.p13 chrX|NW_003871103.3: 2,614,719-3,084,119 , GRCh37.p13 chrX: 154,409,015-154,879,801 TMLHEP1, VBP1, 14 more genes
    nsv7079964copy number variation1nstd229human GRCh38 chrX: 154,810,407-155,540,832 , GRCh37.p13 chrX: 154,038,682-154,770,493 , GRCh37.p13 chrX|NW_003871103.3: 2,244,386-2,974,811 LOC101927830, TWF1P2, 25 more genes
    nsv7056614inversion1nstd229human GRCh38 chrX: 155,268,251-155,309,194 , GRCh37.p13 chrX|NW_003871103.3: 2,702,230-2,743,173 , GRCh37.p13 chrX: 154,497,536-154,538,507 TWF1P2, CLIC2, 1 more genes
    nsv7055893inversion1nstd229human GRCh38 chrX: 155,285,503-155,318,472 , GRCh37.p13 chrX|NW_003871103.3: 2,719,482-2,752,451 , GRCh37.p13 chrX: 154,514,794-154,547,784 PHF10P1, TWF1P2, 1 more genes
    nsv7055504inversion1nstd229human GRCh38 chrX: 155,109,618-155,387,932 , GRCh37.p13 chrX: 154,337,893-154,617,581 , GRCh37.p13 chrX|NW_003871103.3: 2,543,597-2,821,911 VBP1, TMLHEP1, 9 more genes
    nsv7051837inversion1nstd229human GRCh38 chrX: 154,878,232-155,544,292 , GRCh37.p13 chrX|NW_003871103.3: 2,312,211-2,978,271 , GRCh37.p13 chrX: 154,106,507-154,773,953 EEF1A1P31, F8A3, 23 more genes
    nsv7047528inversion1nstd229human GRCh38 chrX: 154,890,289-155,397,026 , GRCh37.p13 chrX|NW_003871103.3: 2,324,268-2,831,005 , GRCh37.p13 chrX: 154,118,564-154,626,687 CLIC2, BRCC3, 15 more genes
    nsv7046188inversion1nstd229human GRCh38 chrX: 152,545,731-155,311,806 , GRCh37.p13 chrX: 151,734,490-154,541,118 , GRCh37.p13 chrX|NW_003871103.3: 1-2,745,785 TEX28, SSR4, 133 more genes
    nsv7043422inversion1nstd229human GRCh38 chrX: 154,891,982-155,401,003 , GRCh37.p13 chrX: 154,120,257-154,630,664 , GRCh37.p13 chrX|NW_003871103.3: 2,325,961-2,834,982 MIR1184-2, EEF1A1P31, 15 more genes
    nsv7043394inversion1nstd229human GRCh38 chrX: 154,722,824-155,408,289 , GRCh37.p13 chrX|NW_003871103.3: 2,156,803-2,842,268 , GRCh37.p13 chrX: 153,951,099-154,637,950 PHF10P1, F8A1, 26 more genes
    nsv7038509inversion1nstd229human GRCh38 chrX: 155,124,718-155,392,395 , GRCh37.p13 chrX|NW_003871103.3: 2,558,697-2,826,374 , GRCh37.p13 chrX: 154,352,993-154,622,044 BRCC3, VBP1, 9 more genes
    nsv7038163inversion1nstd229human GRCh38 chrX: 154,895,211-155,297,356 , GRCh37.p13 chrX|NW_003871103.3: 2,329,190-2,731,335 , GRCh37.p13 chrX: 154,123,486-154,526,653 MTCP1, RAB39B, 10 more genes
    nsv6637137copy number variation1nstd102humanPathogenic GRCh37 chrX: 154,112,020-154,617,577 , GRCh38.p12 chrX: 154,883,745-155,387,928 MIR1184-1, BRCC3, 18 more genes
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