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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6910599copy number variation1nstd229human GRCh38 chr11: 73,376,731-73,384,112 , GRCh37.p13 chr11: 73,087,776-73,095,157 RELT
    nsv4987276copy number variation1nstd200human GRCh38 chr11: 73,370,904-73,377,118 , GRCh37.p13 chr11: 73,081,949-73,088,163 RELT
    nsv4833526copy number variation1nstd200human GRCh37 chr11: 73,081,949-73,088,163 , GRCh38.p12 chr11: 73,370,904-73,377,118 RELT
    nsv4987277copy number variation1nstd200human GRCh38 chr11: 73,391,240-73,392,276 , GRCh37.p13 chr11: 73,102,285-73,103,321 RELT
    nsv4847044copy number variation1nstd200human GRCh37 chr11: 73,102,285-73,103,321 , GRCh38.p12 chr11: 73,391,240-73,392,276 RELT
    nsv1126300copy number variation1nstd106human GRCh37 chr11: 73,087,300-73,088,000 , GRCh38.p12 chr11: 73,376,255-73,376,955 RELT
    esv3375921copy number variation8estd59human NCBI36 chr11: 72,779,502-72,782,300 , GRCh37.p13 chr11: 73,101,854-73,104,652 , GRCh38.p12 chr11: 73,390,809-73,393,607 RELT
    esv3786194copy number variation1estd192human GRCh37 chr11: 73,104,051-73,104,257 , GRCh38.p12 chr11: 73,393,006-73,393,212 RELT
    nsv4193013copy number variation1nstd166human GRCh37.p13 chr11: 73,093,500-73,100,000 , GRCh38.p12 chr11: 73,382,455-73,388,955 RELT
    esv2336600insertion1estd194human NCBI36 chr11: 72,782,491-72,782,491 , GRCh37.p13 chr11: 73,104,843-73,104,843 , GRCh38.p12 chr11: 73,393,798-73,393,798 RELT
    nsv1596110short tandem repeat14nstd128human GRCh37 chr11: 73,088,315-73,088,338 , GRCh38.p12 chr11: 73,377,270-73,377,293 RELT
    nsv1596111short tandem repeat3nstd128human GRCh37 chr11: 73,088,727-73,088,746 , GRCh38.p12 chr11: 73,377,682-73,377,701 RELT
    nsv1593418short tandem repeat1nstd128human GRCh37 chr11: 73,088,121-73,088,140 , GRCh38.p12 chr11: 73,377,076-73,377,095 RELT
    nsv1594028short tandem repeat6nstd128human GRCh37 chr11: 73,097,993-73,098,008 , GRCh38.p12 chr11: 73,386,948-73,386,963 RELT
    nsv1593419short tandem repeat1nstd128human GRCh37 chr11: 73,089,724-73,089,735 , GRCh38.p12 chr11: 73,378,679-73,378,690 RELT
    nsv4208087copy number variation1nstd166human GRCh37.p13 chr11: 73,108,836-73,109,562 , GRCh38.p12 chr11: 73,397,791-73,398,517 RELT, FAM168A
    nsv897911copy number variation1nstd71human NCBI36 chr11: 72,721,999-72,785,924 , GRCh37.p13 chr11: 73,044,351-73,108,276 , GRCh38.p12 chr11: 73,333,306-73,397,231 ARHGEF17, RELT
    nsv6917182copy number variation1nstd229human GRCh38 chr11: 73,367,584-73,384,436 , GRCh37.p13 chr11: 73,078,629-73,095,481 RELT, ARHGEF17
    nsv943383copy number variation1nstd84human GRCh37 chr11: 73,105,283-73,118,689 , GRCh38.p12 chr11: 73,394,238-73,407,644 FAM168A, RELT
    nsv825993copy number variation1nstd67human NCBI36 chr11: 72,706,857-72,769,577 , GRCh37.p13 chr11: 73,029,209-73,091,929 , GRCh38.p12 chr11: 73,318,164-73,380,884 ARHGEF17, RELT
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