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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928204copy number variation1nstd209human GRCh38 chr19: 55,821,608-55,821,719 , GRCh37.p13 chr19: 56,332,974-56,333,085 NLRP11
    nsv5885090copy number variation1nstd209human GRCh38 chr19: 55,828,467-55,830,216 , GRCh37.p13 chr19: 56,339,833-56,341,582 NLRP11
    nsv5871970copy number variation1nstd209human GRCh38 chr19: 55,796,797-55,797,896 , GRCh37.p13 chr19: 56,308,163-56,309,262 NLRP11
    nsv5870127copy number variation1nstd209human GRCh38 chr19: 55,790,291-55,791,490 , GRCh37.p13 chr19: 56,301,657-56,302,856 NLRP11
    nsv5709467mobile element insertion1nstd211human GRCh38 chr19: 55,802,034-55,802,034 , GRCh37.p13 chr19: 56,313,400-56,313,400 NLRP11
    nsv5698168mobile element insertion1nstd211human GRCh38 chr19: 55,830,615-55,830,615 , GRCh37.p13 chr19: 56,341,981-56,341,981 NLRP11
    nsv5647767insertion1nstd207human GRCh38 chr19: 55,831,098-55,831,098 , GRCh37.p13 chr19: 56,342,464-56,342,464 NLRP11
    nsv5604264copy number variation1nstd207human GRCh38 chr19: 55,793,115-55,795,722 , GRCh37.p13 chr19: 56,304,481-56,307,088 NLRP11
    nsv5584642copy number variation1nstd207human GRCh38 chr19: 55,821,608-55,821,719 , GRCh37.p13 chr19: 56,332,974-56,333,085 NLRP11
    nsv5532246copy number variation1nstd206human GRCh38 chr19: 55,796,708-55,798,055 , GRCh37.p13 chr19: 56,308,074-56,309,421 NLRP11
    nsv5528327copy number variation1nstd206human GRCh38 chr19: 55,793,065-55,795,723 , GRCh37.p13 chr19: 56,304,431-56,307,089 NLRP11
    nsv5526904copy number variation1nstd206human GRCh38 chr19: 55,729,836-55,792,106 , GRCh37.p13 chr19: 56,241,202-56,303,472 NLRP11, NLRP9, 5 more genes
    nsv5526717copy number variation1nstd206human GRCh38 chr19: 55,819,071-55,819,225 , GRCh37.p13 chr19: 56,330,437-56,330,591 NLRP11
    nsv5522503copy number variation1nstd206human GRCh38 chr19: 55,797,953-55,801,689 , GRCh37.p13 chr19: 56,309,319-56,313,055 NLRP11
    nsv5419252mobile element insertion1nstd206human GRCh38 chr19: 55,802,034-55,802,085 , GRCh37.p13 chr19: 56,313,400-56,313,451 NLRP11
    nsv5322586copy number variation1nstd204human GRCh38.p13 chr19: 55,816,789-56,429,675 , GRCh37.p13 chr19: 56,328,155-56,941,044 , ZNF582, 25 more genes
    nsv5295499copy number variation1nstd204human GRCh37.p13 chr19: 56,328,167-56,591,266 , GRCh38.p13 chr19: 55,816,801-56,079,900 NLRP13, NLRP8, 4 more genes
    nsv5294355copy number variation1nstd204human GRCh38.p13 chr19: 55,816,756-55,849,798 , GRCh37.p13 chr19: 56,328,122-56,361,164 NLRP4, NLRP11
    nsv5292239copy number variation1nstd204human GRCh38.p13 chr19: 55,824,601-55,824,900 , GRCh37.p13 chr19: 56,335,967-56,336,266 NLRP11
    nsv5028107copy number variation1nstd200human GRCh38 chr19: 55,807,733-55,808,413 , GRCh37.p13 chr19: 56,319,099-56,319,779 NLRP11
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