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Items: 1 to 20 of 5437

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3071552insertion1nstd90human GRCh37 (hg19) chr10: 6,097,370-6,097,370 , GRCh38 (hg38) chr10: 6,055,407-6,055,407 IL2RA
    nsv3070456mobile element insertion1nstd90human GRCh37 (hg19) chr12: 6,907,384-6,907,639 , GRCh38 (hg38) chr12: 6,798,218-6,798,473 CD4
    nsv3069520insertion1nstd90human GRCh37 (hg19) chr10: 6,097,884-6,097,884 , GRCh38 (hg38) chr10: 6,055,921-6,055,921 IL2RA
    nsv3068711copy number variation1nstd90human GRCh37 (hg19) chr10: 6,097,387-6,097,884 , GRCh38 (hg38) chr10: 6,055,424-6,055,921 IL2RA
    nsv3059187insertion1nstd140human GRCh38 (hg38) chr2: 102,450,207-102,450,208 , GRCh37 (hg19) chr2: 103,066,667-103,066,668 IL18RAP
    nsv3059009copy number variation1nstd140human GRCh37 (hg19) chr12: 6,907,384-6,907,640 , GRCh38 (hg38) chr12: 6,798,218-6,798,474 CD4
    nsv3058842copy number variation1nstd140human GRCh37 (hg19) chr10: 6,097,372-6,097,870 , GRCh38 (hg38) chr10: 6,055,409-6,055,907 IL2RA
    nsv3058839copy number variation1nstd140human GRCh37 (hg19) chr10: 6,073,413-6,073,477 , GRCh38 (hg38) chr10: 6,031,450-6,031,514 IL2RA
    nsv3058233insertion1nstd140human GRCh37 (hg19) chr2: 103,066,667-103,066,668 , GRCh38 (hg38) chr2: 102,450,207-102,450,208 IL18RAP
    nsv3051720copy number variation1nstd140human GRCh38 (hg38) chr10: 6,055,423-6,055,921 , GRCh37 (hg19) chr10: 6,097,386-6,097,884 IL2RA
    nsv2814502insertion1nstd137human GRCh38 (hg38) chr6: 32,584,977-32,584,977 , GRCh37 (hg19) chr6: 32,552,754-32,552,754 HLA-DRB1
    nsv2813341insertion1nstd137human GRCh38 (hg38) chr6: 32,587,382-32,587,382 , GRCh37 (hg19) chr6: 32,555,159-32,555,159 HLA-DRB1
    nsv2813340copy number variation1nstd137human GRCh38 (hg38) chr6: 32,579,835-32,580,152 , GRCh37 (hg19) chr6: 32,547,612-32,547,929 HLA-DRB1
    nsv2804926insertion1nstd137human GRCh38 (hg38) chr2: 102,450,207-102,450,207 , GRCh37 (hg19) chr2: 103,066,667-103,066,667 IL18RAP
    nsv2800911insertion1nstd137human GRCh38 (hg38) chr1: 167,435,269-167,435,269 , GRCh37 (hg19) chr1: 167,404,506-167,404,506 CD247
    nsv2800816insertion1nstd137human GRCh38 (hg38) chr1: 167,435,196-167,435,196 , GRCh37 (hg19) chr1: 167,404,433-167,404,433 CD247
    nsv2796722copy number variation1nstd137human GRCh38 (hg38) chr17: 42,337,875-42,338,134 , GRCh37 (hg19) chr17: 40,489,893-40,490,152 STAT3
    nsv2792578copy number variation1nstd137human GRCh38 (hg38) chr12: 6,798,208-6,798,463 , GRCh37 (hg19) chr12: 6,907,374-6,907,580 CD4
    nsv2792490copy number variation1nstd137human GRCh38 (hg38) chr12: 6,798,219-6,798,474 , GRCh37 (hg19) chr12: 6,907,385-6,907,580 CD4
    nsv2789351copy number variation1nstd137human GRCh38 (hg38) chr10: 6,055,409-6,055,906 , GRCh37 (hg19) chr10: 6,097,372-6,097,869 IL2RA
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