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Items: 1 to 20 of 865

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146434insertion1nstd232human GRCh37.p13 chrX: 154,790,188-154,790,188 , GRCh38.p12 chrX: 155,560,527-155,560,527 TMLHE
    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
    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
    nsv7085677copy number variation1nstd229human GRCh38 chrX: 155,609,276-155,613,223 , GRCh37.p13 chrX|NW_003871103.3: 3,043,255-3,047,202 , GRCh37.p13 chrX: 154,838,937-154,842,884 SPRY3, TMLHE
    nsv7085675copy number variation1nstd229human GRCh38 chrX: 155,577,501-155,580,700 , GRCh37.p13 chrX|NW_003871103.3: 3,011,480-3,014,679 , GRCh37.p13 chrX: 154,807,162-154,810,361 TMLHE
    nsv7085674copy number variation1nstd229human GRCh38 chrX: 155,576,164-155,632,812 , GRCh37.p13 chrX|NW_003871103.3: 3,010,143-3,066,791 , GRCh37.p13 chrX: 154,805,825-154,862,473 TMLHE, SPRY3
    nsv7085673copy number variation1nstd229human GRCh38 chrX: 155,560,559-155,592,493 , GRCh37.p13 chrX: 154,790,220-154,822,154 , GRCh37.p13 chrX|NW_003871103.3: 2,994,538-3,026,472 TMLHE
    nsv7085672copy number variation1nstd229human GRCh38 chrX: 155,560,529-155,573,852 , GRCh37.p13 chrX|NW_003871103.3: 2,994,508-3,007,831 , GRCh37.p13 chrX: 154,790,190-154,803,513 TMLHE
    nsv7085671copy number variation1nstd229human GRCh38 chrX: 155,560,501-155,577,100 , GRCh37.p13 chrX: 154,790,162-154,806,761 , GRCh37.p13 chrX|NW_003871103.3: 2,994,480-3,011,079 TMLHE
    nsv7085670copy number variation1nstd229human GRCh38 chrX: 155,560,501-155,576,200 , GRCh37.p13 chrX: 154,790,162-154,805,861 , GRCh37.p13 chrX|NW_003871103.3: 2,994,480-3,010,179 TMLHE
    nsv7085669copy number variation1nstd229human GRCh38 chrX: 155,560,501-155,575,400 , GRCh37.p13 chrX: 154,790,162-154,805,061 , GRCh37.p13 chrX|NW_003871103.3: 2,994,480-3,009,379 TMLHE
    nsv7085668copy number variation1nstd229human GRCh38 chrX: 155,560,484-155,605,053 , GRCh37.p13 chrX|NW_003871103.3: 2,994,463-3,039,032 , GRCh37.p13 chrX: 154,790,145-154,834,714 TMLHE
    nsv7085667copy number variation1nstd229human GRCh38 chrX: 155,559,601-155,577,200 , GRCh37.p13 chrX: 154,789,262-154,806,861 , GRCh37.p13 chrX|NW_003871103.3: 2,993,580-3,011,179 TMLHE
    nsv7085666copy number variation1nstd229human GRCh38 chrX: 155,559,501-155,576,100 , GRCh37.p13 chrX: 154,789,162-154,805,761 , GRCh37.p13 chrX|NW_003871103.3: 2,993,480-3,010,079 TMLHE
    nsv7085665copy number variation1nstd229human GRCh38 chrX: 155,559,501-155,573,800 , GRCh37.p13 chrX|NW_003871103.3: 2,993,480-3,007,779 , GRCh37.p13 chrX: 154,789,162-154,803,461 TMLHE
    nsv7085664copy number variation1nstd229human GRCh38 chrX: 155,559,401-155,575,200 , GRCh37.p13 chrX|NW_003871103.3: 2,993,380-3,009,179 , GRCh37.p13 chrX: 154,789,062-154,804,861 TMLHE
    nsv7085663copy number variation1nstd229human GRCh38 chrX: 155,558,501-155,576,100 , GRCh37.p13 chrX: 154,788,162-154,805,761 , GRCh37.p13 chrX|NW_003871103.3: 2,992,480-3,010,079 TMLHE
    nsv7085662copy number variation1nstd229human GRCh38 chrX: 155,558,413-155,558,566 , GRCh37.p13 chrX|NW_003871103.3: 2,992,392-2,992,545 , GRCh37.p13 chrX: 154,788,074-154,788,227 TMLHE
    nsv7085661copy number variation1nstd229human GRCh38 chrX: 155,558,301-155,573,800 , GRCh37.p13 chrX|NW_003871103.3: 2,992,280-3,007,779 , GRCh37.p13 chrX: 154,787,962-154,803,461 TMLHE
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