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Items: 1 to 20 of 443

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137157inversion1nstd234human GRCh37 chrX: 31,626,542-82,320,140 , GRCh38.p12 chrX: 31,608,425-83,065,132 ABCB7, ACTG1P10, 775 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
    nsv7080716copy number variation1nstd229human GRCh38 chrX: 37,657,004-37,657,467 , GRCh37.p13 chrX: 37,516,257-37,516,720 , GRCh37.p13 chrX|NW_003871099.1: 368,810-369,273 LANCL3
    nsv7080715copy number variation1nstd229human GRCh38 chrX: 37,655,592-38,492,755 , GRCh37.p13 chrX: 37,669,767-38,352,008 XK, SYTL5, 14 more genes
    nsv7080714copy number variation1nstd229human GRCh38 chrX: 37,654,985-37,661,097 , GRCh37.p13 chrX|NW_003871099.1: 366,791-372,903 , GRCh37.p13 chrX: 37,514,238-37,520,350 LANCL3
    nsv7080713copy number variation1nstd229human GRCh38 chrX: 37,649,636-37,651,557 , GRCh37.p13 chrX: 37,508,889-37,510,810 , GRCh37.p13 chrX|NW_003871099.1: 361,442-363,363 LANCL3
    nsv7080712copy number variation1nstd229human GRCh38 chrX: 37,641,620-37,642,097 , GRCh37.p13 chrX|NW_003871099.1: 353,426-353,903 , GRCh37.p13 chrX: 37,500,873-37,501,350 LANCL3
    nsv7080711copy number variation1nstd229human GRCh38 chrX: 37,637,801-37,641,600 , GRCh37.p13 chrX|NW_003871099.1: 349,607-353,406 , GRCh37.p13 chrX: 37,497,054-37,500,853 LANCL3
    nsv7080710copy number variation1nstd229human GRCh38 chrX: 37,617,274-37,619,679 , GRCh37.p13 chrX: 37,476,527-37,478,932 , GRCh37.p13 chrX|NW_003871099.1: 329,080-331,485 LANCL3
    nsv7080709copy number variation1nstd229human GRCh38 chrX: 37,606,501-37,612,900 , GRCh37.p13 chrX: 37,465,754-37,472,153 , GRCh37.p13 chrX|NW_003871099.1: 318,307-324,706 LANCL3
    nsv7080708copy number variation1nstd229human GRCh38 chrX: 37,606,401-37,612,900 , GRCh37.p13 chrX: 37,465,654-37,472,153 , GRCh37.p13 chrX|NW_003871099.1: 318,207-324,706 LANCL3
    nsv7080707copy number variation1nstd229human GRCh38 chrX: 37,593,379-37,593,906 , GRCh37.p13 chrX|NW_003871099.1: 305,185-305,712 , GRCh37.p13 chrX: 37,452,632-37,453,159 LANCL3
    nsv7080706copy number variation1nstd229human GRCh38 chrX: 37,588,786-37,588,949 , GRCh37.p13 chrX|NW_003871099.1: 300,592-300,755 , GRCh37.p13 chrX: 37,448,039-37,448,202 LANCL3
    nsv7080705copy number variation1nstd229human GRCh38 chrX: 37,567,692-37,612,511 , GRCh37.p13 chrX|NW_003871099.1: 279,498-324,317 , GRCh37.p13 chrX: 37,426,945-37,471,764 LANCL3
    nsv7080703copy number variation1nstd229human GRCh38 chrX: 37,538,269-37,639,210 , GRCh37.p13 chrX|NW_003871099.1: 250,075-351,016 , GRCh37.p13 chrX: 37,397,522-37,498,463 LANCL3, FAM47DP
    nsv7080681copy number variation1nstd229human GRCh38 chrX: 37,362,373-37,675,671 , GRCh37.p13 chrX|NW_003871099.1: 74,179-387,477 , GRCh37.p13 chrX: 37,221,626-37,534,924 FTH1P19, LANCL3, 4 more genes
    nsv7080652copy number variation1nstd229human GRCh38 chrX: 36,821,742-37,799,642 , GRCh37.p13 chrX|NW_003871099.1: 1-511,448 , GRCh37.p13 chrX: 36,839,815-37,658,895 FTHL18P, FAM47DP, 12 more genes
    nsv7037966inversion1nstd229human GRCh38 chrX: 36,986,100-37,575,172 , GRCh37.p13 chrX: 37,004,173-37,434,425 FTH1P19, FAM47C, 9 more genes
    nsv7035480inversion1nstd229human GRCh38 chrX: 37,432,038-37,621,615 , GRCh37.p13 chrX|NW_003871099.1: 143,844-333,421 , GRCh37.p13 chrX: 37,291,291-37,480,868 FAM47DP, LANCL3, 4 more genes
    nsv7032924inversion1nstd229human GRCh38 chrX: 34,355,734-41,258,887 , GRCh37.p13 chrX: 34,373,851-41,118,140 IMPDH1P2, RPL32P36, 81 more genes
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