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Items: 1 to 20 of 259

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3066819insertion1nstd140human GRCh37 (hg19) chrX: 516,333-516,334 , GRCh38 (hg38) chrX|NT_187634.1: 238,951-238,952 , GRCh38 (hg38) chrX|NT_187667.1: 228,091-228,092 , GRCh38 (hg38) chrX: 555,598-555,599 0
    nsv3066818insertion1nstd140human GRCh37 (hg19) chrX: 488,907-488,908 , GRCh38 (hg38) chrX|NT_187634.1: 211,525-211,526 , GRCh38 (hg38) chrX|NT_187667.1: 200,665-200,666 , GRCh38 (hg38) chrX: 528,172-528,173 0
    nsv3066815insertion1nstd140human GRCh37 (hg19) chrX: 418,353-418,354 , GRCh38 (hg38) chrX: 457,618-457,619 , GRCh38 (hg38) chrX|NT_187634.1: 140,971-140,972 , GRCh38 (hg38) chrX|NT_187667.1: 130,111-130,112 0
    nsv3065682copy number variation1nstd140human GRCh37 (hg19) chrX: 541,026-541,079 , GRCh38 (hg38) chrX|NT_187634.1: 263,644-263,697 , GRCh38 (hg38) chrX|NT_187667.1: 252,784-252,837 , GRCh38 (hg38) chrX: 580,291-580,344 0
    nsv3065681copy number variation1nstd140human GRCh37 (hg19) chrX: 445,861-445,959 , GRCh38 (hg38) chrX|NT_187634.1: 168,479-168,577 , GRCh38 (hg38) chrX|NT_187667.1: 157,619-157,717 , GRCh38 (hg38) chrX: 485,126-485,224 0
    nsv3062638insertion1nstd140human GRCh37 (hg19) chrX: 541,309-541,310 , GRCh38 (hg38) chrX: 580,574-580,575 , GRCh38 (hg38) chrX|NT_187634.1: 263,927-263,928 , GRCh38 (hg38) chrX|NT_187667.1: 253,067-253,068 0
    nsv3062633insertion1nstd140human GRCh37 (hg19) chrX: 505,868-505,869 , GRCh38 (hg38) chrX|NT_187667.1: 217,626-217,627 , GRCh38 (hg38) chrX: 545,133-545,134 , GRCh38 (hg38) chrX|NT_187634.1: 228,486-228,487 0
    nsv3061616insertion1nstd140human GRCh37 (hg19) chrX: 526,122-526,123 , GRCh38 (hg38) chrX: 565,387-565,388 , GRCh38 (hg38) chrX|NT_187634.1: 248,740-248,741 , GRCh38 (hg38) chrX|NT_187667.1: 237,880-237,881 0
    nsv3061614insertion1nstd140human GRCh37 (hg19) chrX: 517,915-517,916 , GRCh38 (hg38) chrX|NT_187667.1: 229,673-229,674 , GRCh38 (hg38) chrX: 557,180-557,181 , GRCh38 (hg38) chrX|NT_187634.1: 240,533-240,534 0
    nsv3061612insertion1nstd140human GRCh37 (hg19) chrX: 489,012-489,013 , GRCh38 (hg38) chrX|NT_187634.1: 211,630-211,631 , GRCh38 (hg38) chrX|NT_187667.1: 200,770-200,771 , GRCh38 (hg38) chrX: 528,277-528,278 0
    nsv3061611insertion1nstd140human GRCh37 (hg19) chrX: 488,761-488,762 , GRCh38 (hg38) chrX: 528,026-528,027 , GRCh38 (hg38) chrX|NT_187634.1: 211,379-211,380 , GRCh38 (hg38) chrX|NT_187667.1: 200,519-200,520 0
    nsv3060733copy number variation1nstd140human GRCh37 (hg19) chrX: 466,605-466,836 , GRCh38 (hg38) chrX|NT_187634.1: 189,223-189,454 , GRCh38 (hg38) chrX|NT_187667.1: 178,363-178,594 , GRCh38 (hg38) chrX: 505,870-506,101 0
    nsv3060731copy number variation1nstd140human GRCh37 (hg19) chrX: 448,365-448,423 , GRCh38 (hg38) chrX|NT_187634.1: 170,983-171,041 , GRCh38 (hg38) chrX: 487,630-487,688 , GRCh38 (hg38) chrX|NT_187667.1: 160,123-160,181 0
    nsv3059881insertion1nstd140human GRCh37 (hg19) chrX: 433,489-433,490 , GRCh38 (hg38) chrX: 472,754-472,755 , GRCh38 (hg38) chrX|NT_187634.1: 156,107-156,108 , GRCh38 (hg38) chrX|NT_187667.1: 145,247-145,248 0
    nsv3056732copy number variation1nstd140human GRCh37 (hg19) chrX: 389,768-389,841 , GRCh38 (hg38) chrX|NT_187667.1: 101,526-101,599 , GRCh38 (hg38) chrX: 429,033-429,106 , GRCh38 (hg38) chrX|NT_187634.1: 112,386-112,459 0
    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
    nsv2779145copy number variation2nstd37humanUncertain significance NCBI36 (hg18) chrX: 404,625-459,198 , GRCh37 (hg19) chrX: 484,625-539,198 , GRCh38 (hg38) chrX|NT_187634.1: 207,243-261,816 , GRCh38 (hg38) chrX|NT_187667.1: 196,383-250,956 , GRCh38 (hg38) chrX: 523,890-578,463 0
    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
    nsv2778846copy number variation1nstd37humanBenign GRCh37 (hg19) chrX: 225,816-438,701 , GRCh38 (hg38) chrX: 309,149-477,966 , GRCh38 (hg38) chrX|NT_187667.1: 25,947-150,459 , GRCh38 (hg38) chrX|NT_187634.1: 37,893-161,319 , NCBI36 (hg18) chrX: 165,816-358,701 PPP2R3B, LINC00685, 1 more genes
    nsv2778833copy number variation1nstd37humanBenign GRCh37 (hg19) chrX: 281,527-456,062 , GRCh38 (hg38) chrX|NT_187634.1: 37,893-178,680 , GRCh38 (hg38) chrX|NT_187667.1: 25,947-167,820 , GRCh38 (hg38) chrX: 320,792-495,327 , NCBI36 (hg18) chrX: 201,527-376,062 PPP2R3B, LINC00685
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