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Items: 1 to 20 of 320

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147241copy number variation1nstd232human GRCh37.p13 chrX: 153,713,987-153,714,107 , GRCh38.p12 chrX: 154,485,648-154,485,768 UBL4A, SLC10A3
    nsv7137089copy number variation1nstd102humannot provided GRCh37 chrX: 153,566,798-153,748,208 , GRCh38.p12 chrX: 154,338,448-154,519,994 SLC10A3, FLNA, 16 more genes
    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
    nsv7098354copy number variation1nstd102humanUncertain significance GRCh37 chrX: 153,585,782-153,775,961 , GRCh38.p12 chrX: 154,357,414-154,547,746 UBL4A, GDI1, 17 more genes
    nsv7098245copy number variation3nstd102humanUncertain significance GRCh37 chrX: 153,640,181-153,775,961 , GRCh38.p12 chrX: 154,411,844-154,547,746 TAFAZZIN, FAM3A, 13 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
    nsv7079918copy number variation1nstd229human GRCh38 chrX: 154,461,119-154,608,559 , GRCh37.p13 chrX: 153,689,459-153,836,812 , GRCh37.p13 chrX|NW_003871103.3: 1,895,098-2,042,538 UBL4A, FAM3A, 9 more genes
    nsv7079913copy number variation1nstd229human GRCh38 chrX: 154,457,901-154,488,700 , GRCh37.p13 chrX: 153,686,241-153,717,039 , GRCh37.p13 chrX|NW_003871103.3: 1,891,880-1,922,679 UBL4A, LAGE3, 2 more genes
    nsv7079912copy number variation1nstd229human GRCh38 chrX: 154,457,238-154,596,819 , GRCh37.p13 chrX: 153,685,578-153,825,080 , GRCh37.p13 chrX|NW_003871103.3: 1,891,217-2,030,798 CTAG1A, PLXNA3, 9 more genes
    nsv7079909copy number variation1nstd229human GRCh38 chrX: 154,453,701-154,496,500 , GRCh37.p13 chrX: 153,682,049-153,724,834 , GRCh37.p13 chrX|NW_003871103.3: 1,887,680-1,930,479 LAGE3, SLC10A3, 3 more genes
    nsv7079901copy number variation1nstd229human GRCh38 chrX: 154,428,601-154,488,700 , GRCh37.p13 chrX|NW_003871103.3: 1,862,580-1,922,679 , GRCh37.p13 chrX: 153,656,947-153,717,039 MIR6858, GDI1, 7 more genes
    nsv7079893copy number variation1nstd229human GRCh38 chrX: 154,362,101-154,505,500 , GRCh37.p13 chrX|NW_003871103.3: 1,796,080-1,939,479 , GRCh37.p13 chrX: 153,590,469-153,733,831 PLXNA3, ATP6AP1-DT, 15 more genes
    nsv7079883copy number variation1nstd229human GRCh38 chrX: 154,333,501-154,534,400 , GRCh37.p13 chrX|NW_003871103.3: 1,767,480-1,968,379 , GRCh37.p13 chrX: 153,561,851-153,762,615 G6PD, FLNA, 17 more genes
    nsv7079879copy number variation1nstd229human GRCh38 chrX: 154,324,201-154,504,700 , GRCh37.p13 chrX: 153,552,547-153,733,031 , GRCh37.p13 chrX|NW_003871103.3: 1,758,180-1,938,679 LAGE3, FLNA, 17 more genes
    nsv7079878copy number variation1nstd229human GRCh38 chrX: 154,309,633-154,536,356 , GRCh37.p13 chrX|NW_003871103.3: 1,743,612-1,970,335 , GRCh37.p13 chrX: 153,537,985-153,764,571 SNORA70, LOC105373386, 18 more genes
    nsv7057928inversion1nstd229human GRCh38 chrX: 152,528,769-155,098,506 , GRCh37.p13 chrX: 151,734,490-154,326,781 , GRCh37.p13 chrX|NW_003871103.3: 1-2,532,485 F8, ATP6AP1, 128 more genes
    nsv7051950inversion1nstd229human GRCh38 chrX: 153,712,302-154,514,525 , GRCh37.p13 chrX: 152,977,757-153,742,849 , GRCh37.p13 chrX|NW_003871103.3: 1,146,285-1,948,504 MIR3202-1, LAGE3, 48 more genes
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