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Items: 1 to 20 of 270

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6309114copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,469,557-47,478,800 , GRCh38.p12 chr11: 47,448,005-47,457,248 RAPSN
    nsv7093692copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,467,519-47,469,609 , GRCh38.p12 chr11: 47,445,967-47,448,057 RAPSN
    nsv4682636copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,469,354-47,470,727 , GRCh38.p12 chr11: 47,447,802-47,449,175 RAPSN
    nsv7094087copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,469,354-47,470,726 , GRCh38.p12 chr11: 47,447,802-47,449,174 RAPSN
    nsv3878248copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,459,506-47,460,502 , GRCh38 chr11: 47,437,955-47,438,951 RAPSN
    nsv4681027copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,459,516-47,460,492 , GRCh38.p12 chr11: 47,437,965-47,438,941 RAPSN
    nsv7094171copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,462,700-47,463,483 , GRCh38.p12 chr11: 47,441,149-47,441,931 RAPSN
    nsv7094086copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,460,273-47,460,492 , GRCh38.p12 chr11: 47,438,722-47,438,941 RAPSN
    nsv7094085copy number variation1nstd102humanPathogenic GRCh37 chr11: 47,459,516-47,459,608 , GRCh38.p12 chr11: 47,437,965-47,438,057 RAPSN
    nsv7093490insertion1nstd102humanPathogenic GRCh37 chr11: 47,469,470-47,469,470 , GRCh38 chr11: 47,447,918-47,447,918 RAPSN
    nsv7137101copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 47,459,526-47,460,482 , GRCh38.p12 chr11: 47,437,975-47,438,931 RAPSN
    nsv6898239copy number variation1nstd229human GRCh38 chr11: 61,820,578-61,825,482 , GRCh37.p13 chr11: 61,588,050-61,592,954 FADS2
    nsv6912036copy number variation1nstd229human GRCh38 chr11: 47,437,754-47,440,570 , GRCh37.p13 chr11: 47,459,305-47,462,121 RAPSN
    nsv6473985copy number variation1nstd223human GRCh38 chr11: 61,843,801-61,847,021 , GRCh37.p13 chr11: 61,611,273-61,614,493 FADS2
    nsv6460793copy number variation1nstd223human GRCh38 chr11: 61,858,478-61,859,290 , GRCh37.p13 chr11: 61,625,950-61,626,762 FADS2
    nsv6144107copy number variation1nstd206human GRCh38 chr11: 61,820,813-61,820,886 , GRCh37.p13 chr11: 61,588,285-61,588,358 FADS2
    nsv4666634copy number variation1nstd186human GRCh37 chr11: 61,607,681-61,608,089 , GRCh38.p12 chr11: 61,840,209-61,840,617 FADS2
    nsv6029009copy number variation1nstd212human GRCh38 chr11: 61,824,434-61,824,505 , GRCh37.p13 chr11: 61,591,906-61,591,977 FADS2
    nsv4747134copy number variation1nstd199human GRCh37 chr11: 61,591,871-61,591,988 , GRCh38.p12 chr11: 61,824,399-61,824,516 FADS2
    nsv4979660copy number variation1nstd200human GRCh38 chr11: 61,820,355-61,824,649 , GRCh37.p13 chr11: 61,587,827-61,592,121 FADS2
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