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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5924649copy number variation1nstd209human GRCh38 chr8: 23,057,068-23,057,490 , GRCh37.p13 chr8: 22,914,581-22,915,003 TNFRSF10B
    nsv5916143copy number variation1nstd209human GRCh38 chr8: 23,047,233-23,048,311 , GRCh37.p13 chr8: 22,904,746-22,905,824 TNFRSF10B
    nsv5911807copy number variation1nstd209human GRCh38 chr8: 23,040,363-23,040,421 , GRCh37.p13 chr8: 22,897,876-22,897,934 TNFRSF10B
    nsv5633217insertion1nstd207human GRCh38 chr8: 23,048,162-23,048,162 , GRCh37.p13 chr8: 22,905,675-22,905,675 TNFRSF10B
    nsv5571869copy number variation1nstd207human GRCh38 chr8: 23,040,406-23,040,465 , GRCh37.p13 chr8: 22,897,919-22,897,978 TNFRSF10B
    nsv5565244copy number variation1nstd207human GRCh38 chr8: 23,057,036-23,057,434 , GRCh37.p13 chr8: 22,914,549-22,914,947 TNFRSF10B
    nsv5490827copy number variation1nstd206human GRCh38 chr8: 23,028,058-23,028,112 , GRCh37.p13 chr8: 22,885,571-22,885,625 TNFRSF10B
    nsv5489901copy number variation1nstd206human GRCh38 chr8: 23,056,910-23,057,435 , GRCh37.p13 chr8: 22,914,423-22,914,948 TNFRSF10B
    nsv5483181copy number variation1nstd206human GRCh38 chr8: 23,063,245-23,066,854 , GRCh37.p13 chr8: 22,920,758-22,924,367 TNFRSF10B, LOC286059
    nsv5408565mobile element insertion1nstd206human GRCh38 chr8: 23,018,998-23,018,998 , GRCh37.p13 chr8: 22,876,511-22,876,511 TNFRSF10B, RHOBTB2
    nsv5387741copy number variation2nstd186human GRCh37 chr8: 22,904,710-22,905,895 , GRCh38.p12 chr8: 23,047,197-23,048,382 TNFRSF10B
    nsv5379149translocation1nstd200human GRCh38 chr8: 23,057,435-23,057,435 , GRCh38 chr8: 23,057,083-23,057,083 , GRCh37.p13 chr8: 22,914,948-22,914,948 , GRCh37.p13 chr8: 22,914,596-22,914,596 TNFRSF10B
    nsv5334945translocation1nstd200human GRCh37 chr8: 22,914,596-22,914,596 , GRCh37 chr8: 22,914,948-22,914,948 , GRCh38.p12 chr8: 23,057,435-23,057,435 , GRCh38.p12 chr8: 23,057,083-23,057,083 TNFRSF10B
    nsv5314283copy number variation1nstd204human GRCh38.p13 chr8: 23,057,053-23,057,462 , GRCh37.p13 chr8: 22,914,566-22,914,975 TNFRSF10B
    nsv5302153copy number variation1nstd204human GRCh38.p13 chr8: 23,046,997-23,048,601 , GRCh37.p13 chr8: 22,904,510-22,906,114 TNFRSF10B
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv5183953mobile element insertion1nstd203human GRCh38 chr8: 23,032,539-23,032,555 , GRCh37.p13 chr8: 22,890,052-22,890,068 TNFRSF10B
    nsv5110043mobile element insertion1nstd203human GRCh38 chr8: 23,031,432-23,031,450 , GRCh37.p13 chr8: 22,888,945-22,888,963 TNFRSF10B
    nsv4959675copy number variation1nstd200human GRCh38 chr8: 23,053,248-23,055,333 , GRCh37.p13 chr8: 22,910,761-22,912,846 TNFRSF10B
    nsv4959674copy number variation1nstd200human GRCh38 chr8: 23,043,277-23,045,001 , GRCh37.p13 chr8: 22,900,790-22,902,514 TNFRSF10B
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