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Items: 1 to 20 of 378

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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
    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
    nsv7093362copy number variation1nstd102humanUncertain significance GRCh37 chrX: 154,261,678-154,305,564 , GRCh38.p12 chrX: 155,033,403-155,077,289 CMC4, FUNDC2, 2 more genes
    nsv7080062copy number variation1nstd229human GRCh38 chrX: 155,071,051-155,217,413 , GRCh37.p13 chrX: 154,299,326-154,445,690 , GRCh37.p13 chrX|NW_003871103.3: 2,505,030-2,651,392 MTCP1, BRCC3, 2 more genes
    nsv7080061copy number variation1nstd229human GRCh38 chrX: 155,070,609-155,179,058 , GRCh37.p13 chrX: 154,298,884-154,407,333 , GRCh37.p13 chrX|NW_003871103.3: 2,504,588-2,613,037 BRCC3, CMC4, 1 more genes
    nsv7080060copy number variation1nstd229human GRCh38 chrX: 155,063,457-155,081,261 , GRCh37.p13 chrX|NW_003871103.3: 2,497,436-2,515,240 , GRCh37.p13 chrX: 154,291,732-154,309,536 MTCP1, CMC4, 1 more genes
    nsv7080059copy number variation1nstd229human GRCh38 chrX: 155,058,220-155,065,320 , GRCh37.p13 chrX: 154,286,495-154,293,595 , GRCh37.p13 chrX|NW_003871103.3: 2,492,199-2,499,299 MTCP1, CMC4, 1 more genes
    nsv7080056copy number variation1nstd229human GRCh38 chrX: 155,048,918-155,064,626 , GRCh37.p13 chrX|NW_003871103.3: 2,482,897-2,498,605 , GRCh37.p13 chrX: 154,277,193-154,292,901 FUNDC2, CMC4, 1 more genes
    nsv7080049copy number variation1nstd229human GRCh38 chrX: 155,020,758-155,084,259 , GRCh37.p13 chrX|NW_003871103.3: 2,454,737-2,518,238 , GRCh37.p13 chrX: 154,249,033-154,312,534 CMC4, BRCC3, 3 more genes
    nsv7080048copy number variation1nstd229human GRCh38 chrX: 155,020,081-155,069,420 , GRCh37.p13 chrX|NW_003871103.3: 2,454,060-2,503,399 , GRCh37.p13 chrX: 154,248,356-154,297,695 F8, MTCP1, 3 more genes
    nsv7080046copy number variation1nstd229human GRCh38 chrX: 155,019,201-155,062,668 , GRCh37.p13 chrX: 154,247,476-154,290,943 , GRCh37.p13 chrX|NW_003871103.3: 2,453,180-2,496,647 F8, MTCP1, 2 more genes
    nsv7080045copy number variation1nstd229human GRCh38 chrX: 155,018,683-155,071,130 , GRCh37.p13 chrX: 154,246,958-154,299,405 , GRCh37.p13 chrX|NW_003871103.3: 2,452,662-2,505,109 MTCP1, FUNDC2, 3 more genes
    nsv7080043copy number variation1nstd229human GRCh38 chrX: 155,016,660-155,067,564 , GRCh37.p13 chrX|NW_003871103.3: 2,450,639-2,501,543 , GRCh37.p13 chrX: 154,244,935-154,295,839 F8, MTCP1, 2 more genes
    nsv7080042copy number variation1nstd229human GRCh38 chrX: 155,016,284-155,078,339 , GRCh37.p13 chrX|NW_003871103.3: 2,450,263-2,512,318 , GRCh37.p13 chrX: 154,244,559-154,306,614 FUNDC2, BRCC3, 3 more genes
    nsv7080033copy number variation1nstd229human GRCh38 chrX: 155,000,901-155,116,800 , GRCh37.p13 chrX: 154,229,176-154,345,075 , GRCh37.p13 chrX|NW_003871103.3: 2,434,880-2,550,779 MTCP1, FUNDC2, 3 more genes
    nsv7079996copy number variation1nstd229human GRCh38 chrX: 154,937,993-155,065,997 , GRCh37.p13 chrX|NW_003871103.3: 2,371,972-2,499,976 , GRCh37.p13 chrX: 154,166,268-154,294,272 F8, MTCP1, 2 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
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