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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3063963copy number variation1nstd140human GRCh38 (hg38) chrX: 636,553-636,729 , GRCh37 (hg19) chrX: 597,288-597,464 SHOX
    nsv3051866insertion1nstd140human GRCh38 (hg38) chrX: 648,051-648,052 , GRCh37 (hg19) chrX: 608,786-608,787 SHOX
    nsv3051565copy number variation1nstd140human GRCh38 (hg38) chrX: 655,569-655,636 , GRCh37 (hg19) chrX: 616,304-616,371 SHOX
    nsv2820879copy number variation1nstd137human GRCh38 (hg38) chrX: 636,518-636,697 , GRCh37 (hg19) chrX: 597,253-597,432 SHOX
    nsv2820878insertion1nstd137human GRCh38 (hg38) chrX: 626,555-626,555 , GRCh37 (hg19) chrX: 587,290-587,290 SHOX
    nsv2820767copy number variation1nstd137human GRCh38 (hg38) chrX: 648,103-648,184 , GRCh37 (hg19) chrX: 608,838-608,919 SHOX
    nsv2820766copy number variation1nstd137human GRCh38 (hg38) chrX: 647,770-647,851 , GRCh37 (hg19) chrX: 608,505-608,586 SHOX
    nsv2820765copy number variation1nstd137human GRCh38 (hg38) chrX: 647,196-647,605 , GRCh37 (hg19) chrX: 607,931-608,340 SHOX
    nsv2820764copy number variation1nstd137human GRCh38 (hg38) chrX: 647,193-647,274 , GRCh37 (hg19) chrX: 607,928-608,009 SHOX
    nsv2820564copy number variation1nstd137human GRCh38 (hg38) chrX: 647,768-647,849 , GRCh37 (hg19) chrX: 608,503-608,584 SHOX
    nsv2819217copy number variation1nstd137human GRCh38 (hg38) chrX: 648,028-648,191 , GRCh37 (hg19) chrX: 608,763-608,926 SHOX
    nsv2819213copy number variation1nstd137human GRCh38 (hg38) chrX: 628,700-628,917 , GRCh37 (hg19) chrX: 589,435-589,652 SHOX
    nsv2819211insertion1nstd137human GRCh38 (hg38) chrX: 625,879-625,879 , GRCh37 (hg19) chrX: 586,614-586,614 SHOX
    nsv2779164copy number variation1nstd37humanPathogenic NCBI36 (hg18) chrX: 439,203-513,493 , GRCh37 (hg19) chrX: 519,203-593,493 , GRCh38 (hg38) chrX: 558,468-632,758 , GRCh38 (hg38) chrX|NT_187634.1: 241,821-284,869 , GRCh38 (hg38) chrX|NT_187667.1: 230,961-274,009 SHOX
    nsv2779068copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 268,480-519,499 , GRCh37 (hg19) chrX: 348,480-599,499 , GRCh38 (hg38) chrX: 387,745-638,764 , GRCh38 (hg38) chrX|NT_187634.1: 71,098-284,869 , GRCh38 (hg38) chrX|NT_187667.1: 60,238-274,009 SHOX
    nsv2779048copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-5,896,155 , GRCh38 (hg38) chrX: 251,879-5,978,114 , NCBI36 (hg18) chrX: 108,546-5,906,155 LINC01546, TRI-GAT1-2, 34 more genes
    nsv2778921copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 70,297-643,638 , GRCh38 (hg38) chrX: 20,297-682,903 , NCBI36 (hg18) chrX: 10,297-563,638 PPP2R3B, LINC00685, 3 more genes
    nsv2778891copy number variation1nstd37humanPathogenic GRCh37 (hg19) chrX: 168,546-155,196,888 , GRCh38 (hg38) chrX: 251,879-155,967,223 , NCBI36 (hg18) chrX: 108,546-154,850,082 GAGE12F, ZBTB33, 1112 more genes
    nsv2778279copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrX: 350,431-154,913,754 , GRCh37 (hg19) chrX: 430,431-155,260,560 , GRCh38 (hg38) chrX: 469,696-156,030,895 GAGE12F, ZBTB33, 1110 more genes
    nsv2778213copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chrY: 539,179-741,993 , GRCh37 (hg19) chrY: 569,179-771,993 , GRCh38 (hg38) chrY: 658,444-861,258 SHOX
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