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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093682copy number variation1nstd102humanUncertain significance GRCh37 chr11: 30,253,450-32,460,464 , GRCh38.p12 chr11: 30,231,903-32,438,918 ARL14EP, PAX6, 28 more genes
    nsv7070958inversion1nstd229human GRCh38 chr11: 29,042,371-30,786,159 , GRCh37.p13 chr11: 29,063,918-30,807,706 LOC100421558, LINC02546, 18 more genes
    nsv7070141inversion1nstd229human GRCh38 chr11: 29,327,534-32,366,322 , GRCh37.p13 chr11: 29,349,081-32,387,868 PAX6, PAUPAR, 35 more genes
    nsv6912301copy number variation1nstd229human GRCh38 chr11: 30,016,986-30,315,412 , GRCh37.p13 chr11: 30,038,533-30,336,959 LOC107984321, ARL14EP-DT, 2 more genes
    nsv6901489copy number variation1nstd229human GRCh38 chr11: 29,922,234-30,610,383 , GRCh37.p13 chr11: 29,943,781-30,631,930 KCNA4, FSHB, 8 more genes
    nsv6901266copy number variation1nstd229human GRCh38 chr11: 30,189,231-30,248,478 , GRCh37.p13 chr11: 30,210,778-30,270,025 ARL14EP-DT, FSHB
    nsv6450291copy number variation1nstd223human GRCh38 chr11: 30,119,133-31,636,993 , GRCh37.p13 chr11: 30,140,680-31,658,540 RPL12P30, LOC105376611, 14 more genes
    nsv6315083copy number variation1nstd102humannot provided GRCh37 chr11: 27,547,893-31,656,604 , GRCh38.p12 chr11: 27,526,346-31,635,057 KIF18A, ARL14EP-DT, 41 more genes
    nsv6290858copy number variation1nstd102humanLikely benign GRCh37 chr11: 30,217,502-30,293,769 , GRCh38.p12 chr11: 30,195,955-30,272,222 FSHB, ARL14EP-DT
    nsv6247927mobile element insertion1nstd215human GRCh38 chr11: 30,234,627-30,234,627 , GRCh37.p13 chr11: 30,256,174-30,256,174 FSHB, ARL14EP-DT
    nsv6132262copy number variation1nstd213human GRCh37 chr11: 29,810,000-30,290,001 , GRCh38.p12 chr11: 29,788,453-30,268,454 FSHB, KCNA4, 3 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729700copy number variation1nstd102humanLikely benign GRCh37 chr11: 30,216,157-30,276,703 , GRCh38.p12 chr11: 30,194,610-30,255,156 FSHB, ARL14EP-DT
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4674824copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344 SNORA88, LINC02729, 305 more genes
    nsv4456492copy number variation1nstd102humanPathogenic GRCh37 chr11: 30,217,030-30,276,703 , GRCh38.p12 chr11: 30,195,483-30,255,156 ARL14EP-DT, FSHB
    nsv4455873copy number variation1nstd102humanPathogenic GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097 DNAJC24, LOC102723568, 153 more genes
    nsv4202384copy number variation1nstd166human GRCh37.p13 chr11: 30,210,781-30,270,027 , GRCh38.p12 chr11: 30,189,234-30,248,480 ARL14EP-DT, FSHB
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