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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112660copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 11,403,560-11,853,760 , GRCh38.p12 chr8: 11,546,051-11,996,251 , GRCh38.p12 chr8|NW_018654717.1: 1,351,766-1,802,047 BLK, CTSB, 19 more genes
    nsv5850170copy number variation1nstd209human GRCh38 chr8: 11,768,376-11,796,016 , GRCh37.p13 chr8: 11,625,885-11,653,525 FDFT1, NEIL2, 2 more genes
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5584099copy number variation1nstd207human GRCh38 chr8: 11,782,763-11,782,889 , GRCh37.p13 chr8: 11,640,272-11,640,398 NEIL2
    nsv5475718copy number variation1nstd206human GRCh38 chr8: 11,784,669-11,787,855 , GRCh37.p13 chr8: 11,642,178-11,645,364 NEIL2, LOC105379243
    nsv5308189copy number variation1nstd204human GRCh38.p13 chr8: 11,769,255-11,945,285 , GRCh37.p13 chr8: 11,626,764-11,802,794 CTSB, FDFT1, 7 more genes
    nsv5241060copy number variation1nstd204human GRCh38.p13 chr8: 11,769,026-11,825,186 , GRCh37.p13 chr8: 11,626,535-11,682,695 FDFT1, SUB1P1, 2 more genes
    nsv5200364copy number variation1nstd102humanPathogenic GRCh37 chr8: 176,814-43,396,776 , GRCh38.p12 chr8: 226,814-43,541,633 LOC100130612, XPO7, 770 more genes
    nsv4969056copy number variation1nstd200human GRCh38 chr8: 11,172,080-11,973,898 , GRCh37.p13 chr8: 11,029,589-11,831,407 NEIL2, MTMR9, 28 more genes
    nsv4959115copy number variation1nstd200human GRCh38 chr8: 11,769,264-11,945,278 , GRCh37.p13 chr8: 11,626,773-11,802,787 CTSB, FDFT1, 7 more genes
    nsv4959114copy number variation1nstd200human GRCh38 chr8: 11,768,840-11,780,100 , GRCh37.p13 chr8: 11,626,349-11,637,609 NEIL2
    nsv4825617copy number variation1nstd200human GRCh37 chr8: 11,029,589-11,831,407 , GRCh38.p12 chr8: 11,172,080-11,973,898 , GRCh38.p12 chr8|NW_018654717.1: 1,374,123-2,174,821 BLK, TDH-AS1, 28 more genes
    nsv4821108copy number variation1nstd200human GRCh37 chr8: 11,626,773-11,802,787 , GRCh38.p12 chr8: 11,769,264-11,945,278 , GRCh38.p12 chr8|NW_018654717.1: 1,402,751-1,578,835 CTSB, FDFT1, 7 more genes
    nsv4821107copy number variation1nstd200human GRCh37 chr8: 11,626,349-11,637,609 , GRCh38.p12 chr8: 11,768,840-11,780,100 , GRCh38.p12 chr8|NW_018654717.1: 1,567,998-1,579,260 NEIL2
    nsv4760008inversion1nstd199human GRCh37 chr8: 7,992,189-12,394,523 , GRCh38.p12 chr8: 8,134,667-12,537,014 , GRCh38.p12 chr8|NW_018654717.1: 1,050,681-5,213,250 , BLK, 129 more genes
    nsv4746886copy number variation1nstd199human GRCh37 chr8: 11,640,291-11,640,417 , GRCh38.p12 chr8: 11,782,782-11,782,908 , GRCh38.p12 chr8|NW_018654717.1: 1,565,190-1,565,316 NEIL2
    nsv4730173inversion85nstd198human GRCh38 chr8: 7,052,376-12,760,459 , GRCh37.p13 chr8: 6,909,898-12,617,968 , BLK, 214 more genes
    nsv4728933copy number variation1nstd102humanPathogenic GRCh37 chr8: 11,147,024-11,945,856 , GRCh38.p12 chr8: 11,289,515-12,088,347 , GRCh38.p12 chr8|NW_018654717.1: 1,280,656-2,057,334 LOC105379241, DEFB136, 35 more genes
    nsv4684267copy number variation1nstd102humanPathogenic GRCh37 chr8: 7,881,478-11,860,845 , GRCh38.p12 chr8|NW_018654717.1: 1,344,700-5,214,290 , GRCh38.p12 chr8: 8,023,956-12,003,336 SUB1P1, DEFB135, 100 more genes
    nsv4675488copy number variation1nstd102humanLikely benign GRCh37 chr8: 11,641,710-11,793,548 , GRCh38.p12 chr8: 11,784,201-11,936,039 , GRCh38.p12 chr8|NW_018654717.1: 1,411,993-1,563,897 CTSB, FDFT1, 6 more genes
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