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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137724copy number variation1nstd102humanPathogenic GRCh37 chr1: 16,785,250-23,491,592 , GRCh38.p12 chr1: 16,458,755-23,165,099 PADI1, RPS15AP6, 176 more genes
    nsv5883934copy number variation1nstd209human GRCh38 chr1: 16,479,843-16,479,978 , GRCh37.p13 chr1: 16,806,338-16,806,473 CROCCP3
    nsv5874690copy number variation1nstd209human GRCh38 chr1: 16,479,184-16,479,489 , GRCh37.p13 chr1: 16,805,679-16,805,984 CROCCP3
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5872548copy number variation1nstd209human GRCh38 chr1: 16,483,368-16,485,098 , GRCh37.p13 chr1: 16,809,863-16,811,593 CROCCP3
    nsv5868990copy number variation1nstd209human GRCh38 chr1: 16,480,201-16,482,347 , GRCh37.p13 chr1: 16,806,696-16,808,842 CROCCP3
    nsv5828599copy number variation1nstd209human GRCh38 chr1: 16,483,340-16,485,091 , GRCh37.p13 chr1: 16,809,835-16,811,586 CROCCP3
    nsv5828510copy number variation1nstd209human GRCh38 chr1: 16,480,165-16,481,464 , GRCh37.p13 chr1: 16,806,660-16,807,959 CROCCP3
    nsv5614695insertion1nstd207human GRCh38 chr1: 16,479,843-16,479,843 , GRCh37.p13 chr1: 16,806,338-16,806,338 CROCCP3
    nsv5569651copy number variation1nstd207human GRCh38 chr1: 16,483,368-16,485,098 , GRCh37.p13 chr1: 16,809,863-16,811,593 CROCCP3
    nsv5560911sequence alteration1nstd206human GRCh38 chr1: 16,483,139-16,940,239 , GRCh37.p13 chr1: 16,809,634-17,266,734 , RNU1-4, 35 more genes
    nsv5433529copy number variation1nstd206human GRCh38 chr1: 16,483,370-16,485,099 , GRCh37.p13 chr1: 16,809,865-16,811,594 CROCCP3
    nsv5433136copy number variation1nstd206human GRCh38 chr1: 16,466,783-16,466,859 , GRCh37.p13 chr1: 16,793,278-16,793,354 CROCCP3, LINC01772
    nsv5432346copy number variation1nstd206human GRCh38 chr1: 16,487,584-16,494,265 , GRCh37.p13 chr1: 16,814,079-16,820,760 CROCCP3
    nsv5355226translocation1nstd200human GRCh38 chr1: 16,484,305-16,484,305 , GRCh38 chr1: 16,484,381-16,484,381 , GRCh37.p13 chr1: 16,810,876-16,810,876 , GRCh37.p13 chr1: 16,810,800-16,810,800 CROCCP3
    nsv5288520copy number variation1nstd204human GRCh38.p13 chr1: 16,483,365-16,485,104 , GRCh37.p13 chr1: 16,809,860-16,811,599 CROCCP3
    nsv5286116copy number variation1nstd204human GRCh38.p13 chr1: 16,480,169-16,482,248 , GRCh37.p13 chr1: 16,806,664-16,808,743 CROCCP3
    nsv5216009copy number variation1nstd204human GRCh38.p13 chr1: 16,483,401-16,485,100 , GRCh37.p13 chr1: 16,809,896-16,811,595 CROCCP3
    nsv5210821copy number variation1nstd204human GRCh38.p13 chr1: 16,483,340-16,485,091 , GRCh37.p13 chr1: 16,809,835-16,811,586 CROCCP3
    nsv5210544copy number variation1nstd204human GRCh38.p13 chr1: 16,479,915-16,482,214 , GRCh37.p13 chr1: 16,806,410-16,808,709 CROCCP3
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