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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3068874insertion1nstd90human GRCh37 (hg19) chr3: 197,245,728-197,245,728 , GRCh38 (hg38) chr3: 197,518,857-197,518,857 , GRCh38 (hg38) chr3|NT_187534.1: 40,026-40,026 BDH1
    nsv3068585insertion1nstd90human GRCh37 (hg19) chr19: 50,205,115-50,205,116 , GRCh38 (hg38) chr19: 49,701,858-49,701,859 CPT1C
    nsv3068516insertion1nstd90human GRCh37 (hg19) chr17: 29,659,946-29,659,946 , GRCh38 (hg38) chr17: 31,332,928-31,332,928 NF1
    nsv3067496copy number variation1nstd90human GRCh37 (hg19) chr5: 142,935,381-142,935,692 , GRCh38 (hg38) chr5: 143,555,816-143,556,127 NR3C1
    nsv3066101insertion1nstd140human GRCh37 (hg19) chr17: 29,662,321-29,662,322 , GRCh38 (hg38) chr17: 31,335,303-31,335,304 NF1
    nsv3065406copy number variation1nstd140human GRCh37 (hg19) chr4: 74,312,306-74,312,370 , GRCh38 (hg38) chr4: 73,446,589-73,446,653 AFP
    nsv3064823insertion1nstd140human GRCh38 (hg38) chr17: 31,335,275-31,335,276 , GRCh37 (hg19) chr17: 29,662,293-29,662,294 NF1
    nsv3060464insertion1nstd140human GRCh37 (hg19) chr20: 43,033,417-43,033,418 , GRCh38 (hg38) chr20: 44,404,777-44,404,778 HNF4A
    nsv3059286copy number variation1nstd140human GRCh37 (hg19) chr17: 29,659,592-29,659,942 , GRCh38 (hg38) chr17: 31,332,574-31,332,924 NF1
    nsv3054573copy number variation1nstd140human GRCh38 (hg38) chr5: 143,555,815-143,556,127 , GRCh37 (hg19) chr5: 142,935,380-142,935,692 NR3C1
    nsv3054541copy number variation1nstd140human GRCh38 (hg38) chr4: 73,446,589-73,446,653 , GRCh37 (hg19) chr4: 74,312,306-74,312,370 AFP
    nsv3045860insertion1nstd140human GRCh38 (hg38) chr5: 143,646,267-143,646,268 , GRCh37 (hg19) chr5: 143,025,832-143,025,833 NR3C1
    nsv3045859insertion1nstd140human GRCh38 (hg38) chr5: 143,631,234-143,631,235 , GRCh37 (hg19) chr5: 143,010,799-143,010,800 NR3C1
    nsv3045159insertion1nstd140human GRCh38 (hg38) chr3: 171,013,724-171,013,725 , GRCh37 (hg19) chr3: 170,731,513-170,731,514 SLC2A2
    nsv3044945insertion1nstd140human GRCh38 (hg38) chr20: 44,404,780-44,404,781 , GRCh37 (hg19) chr20: 43,033,420-43,033,421 HNF4A
    nsv2811956insertion1nstd137human GRCh38 (hg38) chr5: 143,631,225-143,631,225 , GRCh37 (hg19) chr5: 143,010,790-143,010,790 NR3C1
    nsv2811237copy number variation1nstd137human GRCh38 (hg38) chr4: 73,446,588-73,446,651 , GRCh37 (hg19) chr4: 74,312,305-74,312,368 AFP
    nsv2811133insertion2nstd137human GRCh38 (hg38) chr5: 143,433,457-143,433,457 , GRCh37 (hg19) chr5: 142,813,022-142,813,022 NR3C1
    nsv2810532insertion1nstd137human GRCh38 (hg38) chr5: 143,646,267-143,646,267 , GRCh37 (hg19) chr5: 143,025,832-143,025,832 NR3C1
    nsv2810531copy number variation1nstd137human GRCh38 (hg38) chr5: 143,444,853-143,444,902 , GRCh37 (hg19) chr5: 142,824,418-142,824,467 NR3C1
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