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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5927127copy number variation1nstd209human GRCh38 chr9: 136,741,626-136,741,719 , GRCh37.p13 chr9: 139,636,078-139,636,171 LCN10
    nsv5485750copy number variation1nstd206human GRCh38 chr9: 136,735,073-136,751,130 , GRCh37.p13 chr9: 139,629,525-139,645,582 LOC100128593, LCN6, 2 more genes
    nsv5476634copy number variation1nstd206human GRCh38 chr9: 136,742,084-136,742,140 , GRCh37.p13 chr9: 139,636,536-139,636,592 LCN6, LCN10
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5304018copy number variation1nstd204human GRCh37.p13 chr9: 139,629,515-139,645,591 , GRCh38.p13 chr9: 136,735,063-136,751,139 LCN6, LCN10, 2 more genes
    nsv5257656copy number variation1nstd204human GRCh38.p13 chr9: 136,734,647-136,741,132 , GRCh37.p13 chr9: 139,629,099-139,635,584 LCN10
    nsv5251604copy number variation1nstd204human GRCh38.p13 chr9: 136,735,069-136,750,908 , GRCh37.p13 chr9: 139,629,521-139,645,360 LCN6, LCN10, 2 more genes
    nsv5250841copy number variation1nstd204human GRCh38.p13 chr9: 136,735,001-136,752,300 , GRCh37.p13 chr9: 139,629,453-139,646,752 LCN6, LCN10, 2 more genes
    nsv5246206copy number variation1nstd204human GRCh38.p13 chr9: 136,043,001-136,766,200 , GRCh37.p13 chr9: 138,934,847-139,660,652 MIR4674, TMEM250, 37 more genes
    nsv5121888mobile element insertion1nstd203human GRCh38 chr9: 136,736,488-136,736,499 , GRCh37.p13 chr9: 139,630,940-139,630,951 LCN10
    nsv4985874copy number variation1nstd200human GRCh38 chr9: 136,728,676-136,762,286 , GRCh37.p13 chr9: 139,623,128-139,656,738 SNHG7, LCN15, 5 more genes
    nsv4985872copy number variation1nstd200human GRCh38 chr9: 136,710,384-136,754,326 , GRCh37.p13 chr9: 139,604,836-139,648,778 SNHG7, LCN8, 7 more genes
    nsv4985870copy number variation1nstd200human GRCh38 chr9: 136,632,294-136,850,190 , GRCh37.p13 chr9: 139,526,746-139,744,642 CCDC183, PHPT1, 25 more genes
    nsv4985869copy number variation1nstd200human GRCh38 chr9: 136,591,087-136,947,348 , GRCh37.p13 chr9: 139,485,539-139,841,800 LOC102724193, AJM1, 34 more genes
    nsv4985868copy number variation1nstd200human GRCh38 chr9: 136,528,503-136,809,431 , GRCh37.p13 chr9: 139,422,955-139,703,883 LCN6, DIPK1B, 25 more genes
    nsv4973372copy number variation1nstd200human GRCh38 chr9: 136,737,937-136,740,311 , GRCh37.p13 chr9: 139,632,389-139,634,763 LCN10
    nsv4846740copy number variation1nstd200human GRCh37 chr9: 139,629,525-139,645,582 , GRCh38.p12 chr9: 136,735,073-136,751,130 LCN6, LCN10, 2 more genes
    nsv4845671copy number variation1nstd200human GRCh37 chr9: 139,422,955-139,703,883 , GRCh38.p12 chr9: 136,528,503-136,809,431 TMEM141, CCDC183, 25 more genes
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4729067copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,420,166-139,787,562 , GRCh38.p12 chr9: 136,525,714-136,893,110 LCN6, LCN15, 34 more genes
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