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Items: 1 to 20 of 332

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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
    nsv7098598copy number variation2nstd102humanUncertain significance GRCh37 chrX: 152,014,869-153,363,122 , GRCh38.p12 chrX: 152,846,325-154,097,665 AVPR2, HMGN2P48, 56 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
    nsv7079694copy number variation1nstd229human GRCh38 chrX: 152,931,865-152,954,110 , GRCh37.p13 chrX|NW_003871103.3: 365,848-388,093 , GRCh37.p13 chrX: 152,100,409-152,122,654 ZNF185, LOC105373372
    nsv7079693copy number variation1nstd229human GRCh38 chrX: 152,927,971-152,939,381 , GRCh37.p13 chrX|NW_003871103.3: 361,954-373,364 , GRCh37.p13 chrX: 152,096,515-152,107,925 LOC105373372, ZNF185
    nsv7079692copy number variation1nstd229human GRCh38 chrX: 152,927,308-152,931,568 , GRCh37.p13 chrX: 152,095,852-152,100,112 , GRCh37.p13 chrX|NW_003871103.3: 361,291-365,551 ZNF185, LOC105373372
    nsv7079691copy number variation1nstd229human GRCh38 chrX: 152,925,671-152,939,008 , GRCh37.p13 chrX: 152,094,215-152,107,552 , GRCh37.p13 chrX|NW_003871103.3: 359,654-372,991 LOC105373372, ZNF185
    nsv7079690copy number variation1nstd229human GRCh38 chrX: 152,925,375-152,964,407 , GRCh37.p13 chrX: 152,093,919-152,132,951 , GRCh37.p13 chrX|NW_003871103.3: 359,358-398,390 ZNF185, LOC105373372
    nsv7079689copy number variation1nstd229human GRCh38 chrX: 152,925,027-152,933,007 , GRCh37.p13 chrX|NW_003871103.3: 359,010-366,990 , GRCh37.p13 chrX: 152,093,571-152,101,551 LOC105373372, ZNF185
    nsv7079688copy number variation1nstd229human GRCh38 chrX: 152,925,001-152,959,200 , GRCh37.p13 chrX: 152,093,545-152,127,744 , GRCh37.p13 chrX|NW_003871103.3: 358,984-393,183 LOC105373372, ZNF185
    nsv7079687copy number variation1nstd229human GRCh38 chrX: 152,924,949-152,930,830 , GRCh37.p13 chrX: 152,093,493-152,099,374 , GRCh37.p13 chrX|NW_003871103.3: 358,932-364,813 ZNF185, LOC105373372
    nsv7079686copy number variation1nstd229human GRCh38 chrX: 152,923,390-152,936,991 , GRCh37.p13 chrX|NW_003871103.3: 357,373-370,974 , GRCh37.p13 chrX: 152,091,934-152,105,535 LOC105373372, ZNF185
    nsv7079685copy number variation1nstd229human GRCh38 chrX: 152,923,040-152,938,930 , GRCh37.p13 chrX|NW_003871103.3: 357,023-372,913 , GRCh37.p13 chrX: 152,091,584-152,107,474 ZNF185, LOC105373372
    nsv7079684copy number variation1nstd229human GRCh38 chrX: 152,922,567-152,958,414 , GRCh37.p13 chrX: 152,091,111-152,126,958 , GRCh37.p13 chrX|NW_003871103.3: 356,550-392,397 LOC105373372, ZNF185
    nsv7079682copy number variation1nstd229human GRCh38 chrX: 152,907,266-152,950,478 , GRCh37.p13 chrX: 152,075,810-152,119,022 , GRCh37.p13 chrX|NW_003871103.3: 341,249-384,461 LOC105373372, ZNF185
    nsv7079675copy number variation1nstd229human GRCh38 chrX: 152,867,776-152,937,197 , GRCh37.p13 chrX|NW_003871103.3: 301,759-371,180 , GRCh37.p13 chrX: 152,036,320-152,105,741 ZNF185, NSDHL, 1 more genes
    nsv7079666copy number variation1nstd229human GRCh38 chrX: 152,810,766-152,936,044 , GRCh37.p13 chrX|NW_003871103.3: 244,749-370,027 , GRCh37.p13 chrX: 151,979,298-152,104,588 ZNF185, CETN2, 2 more genes
    nsv7079661copy number variation1nstd229human GRCh38 chrX: 152,743,133-152,950,602 , GRCh37.p13 chrX|NW_003871103.3: 177,116-384,585 , GRCh37.p13 chrX: 151,958,440-152,119,146 MAGEA2, ZNF185, 7 more genes
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