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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5564455copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,297,240-139,572,028 , GRCh38.p12 chr9: 136,402,788-136,677,576 LOC105376325, NOTCH1, 14 more genes
    nsv5482821copy number variation1nstd206human GRCh38 chr9: 136,615,141-136,619,930 , GRCh37.p13 chr9: 139,509,593-139,514,382 LINC01451
    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
    nsv5249366copy number variation1nstd204human GRCh38.p13 chr9: 136,536,101-136,611,200 , GRCh37.p13 chr9: 139,430,553-139,505,652 MIR4674, LINC01451, 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
    nsv5242848copy number variation1nstd204human GRCh38.p13 chr9: 136,581,101-136,633,300 , GRCh37.p13 chr9: 139,475,553-139,527,752 LINC01451
    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
    nsv4973364copy number variation1nstd200human GRCh38 chr9: 136,615,141-136,619,930 , GRCh37.p13 chr9: 139,509,593-139,514,382 LINC01451
    nsv4973363copy number variation1nstd200human GRCh38 chr9: 136,613,099-136,616,147 , GRCh37.p13 chr9: 139,507,551-139,510,599 LINC01451
    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
    nsv4837638copy number variation1nstd200human GRCh37 chr9: 139,509,593-139,514,382 , GRCh38.p12 chr9: 136,615,141-136,619,930 LINC01451
    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
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683252copy number variation2nstd102humanUncertain significance GRCh37 chr9: 138,594,085-140,062,314 , GRCh38.p12 chr9: 135,702,239-137,167,862 SAPCD2, MIR3621, 81 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 DPP7, MIR4673, 112 more genes
    nsv4615037copy number variation1nstd183human GRCh37 chr9: 139,512,029-139,575,829 , GRCh38.p12 chr9: 136,617,577-136,681,377 AGPAT2, EGFL7, 5 more genes
    nsv4612627copy number variation1nstd183human GRCh37 chr9: 139,431,355-139,530,152 , GRCh38.p12 chr9: 136,536,903-136,635,700 LINC01451, NALT1, 2 more genes
    nsv4602098copy number variation1nstd183human GRCh37 chr9: 139,326,816-139,632,028 , GRCh38.p12 chr9: 136,432,364-136,737,576 DIPK1B, HSPC324, 17 more genes
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