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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv2593034copy number variation1estd197human NCBI36 chr11: 116,167,244-116,167,244 , GRCh37.p13 chr11: 116,662,034-116,662,034 , GRCh38.p12 chr11: 116,791,318-116,791,318 APOA5
    esv1916748copy number variation1estd194human NCBI36 chr11: 116,167,244-116,167,245 , GRCh37.p13 chr11: 116,662,034-116,662,035 , GRCh38.p12 chr11: 116,791,318-116,791,319 APOA5
    esv1633377insertion1estd22human NCBI36 chr11: 116,166,505-116,166,505 , GRCh37.p13 chr11: 116,661,295-116,661,295 , GRCh38.p12 chr11: 116,790,579-116,790,579 APOA5
    nsv3144612copy number variation2nstd151human GRCh37 chr11: 116,656,509-116,658,364 , GRCh38.p12 chr11: 116,785,793-116,787,648 APOA5, ZPR1
    nsv3152525copy number variation1nstd151human GRCh37 chr11: 116,660,841-116,693,912 , GRCh38.p12 chr11: 116,790,125-116,823,196 APOA5, APOA4
    nsv7070021inversion1nstd229human GRCh38 chr11: 116,780,316-116,788,160 , GRCh37.p13 chr11: 116,651,032-116,658,876 APOA5, ZPR1
    nsv6910036copy number variation1nstd229human GRCh38 chr11: 116,787,363-116,819,918 , GRCh37.p13 chr11: 116,658,079-116,690,634 APOA5, ZPR1, 1 more genes
    nsv6465487copy number variation1nstd223human GRCh38 chr11: 116,716,184-116,801,139 , GRCh37.p13 chr11: 116,586,900-116,671,855 APOA5, ZPR1, 1 more genes
    nsv3227295copy number variation3nstd152human GRCh38 chr11: 116,770,727-116,809,003 , GRCh37.p13 chr11: 116,641,443-116,679,719 APOA5, ZPR1, 1 more genes
    nsv3966345copy number variation1nstd168human GRCh38 chr11: 116,758,203-116,826,769 , GRCh37.p13 chr11: 116,628,919-116,697,485 APOA5, ZPR1, 2 more genes
    nsv3145964copy number variation1nstd151human GRCh37 chr11: 116,628,479-116,693,912 , GRCh38.p12 chr11: 116,757,763-116,823,196 APOA5, ZPR1, 2 more genes
    nsv3142962copy number variation1nstd151human GRCh37 chr11: 116,656,509-116,701,617 , GRCh38.p12 chr11: 116,785,793-116,830,901 APOA5, APOC3, 2 more genes
    nsv507copy number variation1nstd2human NCBI35 chr11: 116,139,429-116,179,996 , GRCh37.p13 chr11: 116,634,219-116,674,786 , GRCh38.p12 chr11: 116,763,503-116,804,070 APOA5, ZPR1, 1 more genes
    esv3802661copy number variation1estd192human GRCh37 chr11: 116,570,956-116,676,536 , GRCh38.p12 chr11: 116,700,240-116,805,820 APOA5, ZPR1, 1 more genes
    nsv6913541copy number variation1nstd229human GRCh38 chr11: 116,693,198-116,792,330 , GRCh37.p13 chr11: 116,563,914-116,663,046 APOA5, ZPR1, 1 more genes
    nsv6908872copy number variation1nstd229human GRCh38 chr11: 116,753,087-116,792,351 , GRCh37.p13 chr11: 116,623,803-116,663,067 APOA5, BUD13, 1 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 APOA5, FAUP4, 2031 more genes
    nsv4455554copy number variation1nstd102humanPathogenic GRCh37 chr11: 104,101,411-116,680,918 , GRCh38.p12 chr11: 104,230,683-116,810,202 APOA5, LINC02732, 198 more genes
    nsv7093918copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr11: 116,660,844-117,870,356 , GRCh38.p12 chr11: 116,790,128-117,999,641 APOA5, PAFAH1B2, 26 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 APOA5, LOC105376598, 2842 more genes
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