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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3157103copy number variation1nstd151human GRCh37 (hg19) chr15: 43,132,555-43,170,820 , GRCh38 (hg38) chr15: 42,840,357-42,878,622 TTBK2
    nsv3155076copy number variation3nstd151human GRCh37 (hg19) chr15: 43,093,163-43,093,638 , GRCh38 (hg38) chr15: 42,800,965-42,801,440 TTBK2
    nsv3153674copy number variation1nstd151human GRCh37 (hg19) chr15: 43,067,330-43,678,533 , GRCh38 (hg38) chr15: 42,775,132-43,386,335 TGM7, ZSCAN29, 9 more genes
    nsv3149964copy number variation1nstd151human GRCh37 (hg19) chr15: 43,164,806-43,256,246 , GRCh38 (hg38) chr15: 42,872,608-42,964,048 TTBK2, UBR1
    nsv3144113copy number variation1nstd151human GRCh37 (hg19) chr15: 43,132,555-43,281,170 , GRCh38 (hg38) chr15: 42,840,357-42,988,972 TTBK2, UBR1
    nsv3143181copy number variation1nstd151human GRCh37 (hg19) chr15: 43,017,684-43,170,820 , GRCh38 (hg38) chr15: 42,725,486-42,878,622 TTBK2, CDAN1
    nsv3140973copy number variation5nstd151human GRCh37 (hg19) chr15: 43,170,744-43,170,820 , GRCh38 (hg38) chr15: 42,878,546-42,878,622 TTBK2
    nsv3140812copy number variation1nstd151human GRCh37 (hg19) chr15: 43,164,806-43,276,196 , GRCh38 (hg38) chr15: 42,872,608-42,983,998 TTBK2, UBR1
    nsv3104825mobile element insertion1nstd144human GRCh37 (hg19) chr15: 43,157,103-43,157,103 , GRCh38 (hg38) chr15: 42,864,905-42,864,905 TTBK2
    nsv2786043copy number variation1nstd132human NCBI36 (hg18) chr15: 40,904,198-41,179,367 , GRCh37 (hg19) chr15: 43,116,906-43,392,075 , GRCh38 (hg38) chr15: 42,824,708-43,099,877 TTBK2, UBR1
    nsv2785262copy number variation1nstd132human NCBI36 (hg18) chr15: 40,891,698-41,232,597 , GRCh37 (hg19) chr15: 43,104,406-43,445,305 , GRCh38 (hg38) chr15: 42,812,208-43,153,107 TTBK2, UBR1, 1 more genes
    nsv2783142copy number variation1nstd132human NCBI36 (hg18) chr15: 40,997,322-41,327,409 , GRCh37 (hg19) chr15: 43,210,030-43,540,117 , GRCh38 (hg38) chr15: 42,917,832-43,247,919 TTBK2, UBR1, 4 more genes
    nsv2782529copy number variation2nstd132human NCBI36 (hg18) chr15: 40,904,198-41,232,597 , GRCh37 (hg19) chr15: 43,116,906-43,445,305 , GRCh38 (hg38) chr15: 42,824,708-43,153,107 TTBK2, UBR1, 1 more genes
    nsv2779140copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 21,173,967-100,338,915 , GRCh37 (hg19) chr15: 23,622,526-102,521,392 , GRCh38 (hg38) chr15: 23,377,379-101,981,189 NR2E3, SNORD116-1, 882 more genes
    nsv2778543copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 18,323,354-100,338,915 , GRCh37 (hg19) chr15: 20,063,340-102,521,392 , GRCh38 (hg38) chr15: 19,858,087-101,981,189 NR2E3, SNORD116-1, 913 more genes
    nsv2777568copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 41,689,327-52,446,981 , GRCh38 (hg38) chr15: 41,397,129-52,154,784 , NCBI36 (hg18) chr15: 39,476,619-50,234,273 MIR147B, GABPB1-AS1, 132 more genes
    nsv2777189copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 26,996,912-100,338,915 , GRCh37 (hg19) chr15: 29,209,620-102,521,392 , GRCh38 (hg38) chr15: 28,917,417-101,981,189 NR2E3, FAM138E, 757 more genes
    nsv2776267copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 20,733,395-102,511,616 , GRCh38 (hg38) chr15: 20,528,156-101,971,413 , NCBI36 (hg18) chr15: 18,993,409-100,329,139 NR2E3, SNORD116-1, 908 more genes
    nsv2775831copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr15: 22,770,422-102,429,112 , GRCh38 (hg38) chr15: 22,358,243-101,888,909 , NCBI36 (hg18) chr15: 20,321,786-100,246,635 NR2E3, SNORD116-1, 886 more genes
    nsv2775587copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr15: 40,953,625-41,139,254 , GRCh37 (hg19) chr15: 43,166,333-43,351,962 , GRCh38 (hg38) chr15: 42,874,135-43,059,764 TTBK2, UBR1
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