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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5381736copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,764,148-141,066,491 , GRCh38.p12 chr9: 136,869,696-138,172,039 PTGDS, LCN12, 63 more genes
    nsv5334101translocation1nstd200human GRCh37 chr9: 140,138,412-140,138,412 , GRCh37 chr9: 140,138,462-140,138,462 , GRCh38.p12 chr9: 137,243,960-137,243,960 , GRCh38.p12 chr9: 137,244,010-137,244,010 CIMIP2A, TUBB4B
    nsv5243007copy number variation1nstd204human GRCh38.p13 chr9: 136,845,001-137,273,000 , GRCh37.p13 chr9: 139,739,453-140,167,452 ENTPD2, LINC02908, 43 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
    nsv4728942copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,776,707-140,234,193 , GRCh38.p12 chr9: 136,882,255-137,339,741 GRIN1, CYSRT1, 42 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
    nsv4683512copy number variation1nstd102humanPathogenic GRCh37 chr9: 140,033,919-140,729,425 , GRCh38.p12 chr9: 137,139,467-137,834,973 CIMIP2A, ENTPD8, 34 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
    nsv4601138copy number variation1nstd183human GRCh37 chr9: 140,129,040-140,139,146 , GRCh38.p12 chr9: 137,234,588-137,244,694 SLC34A3, TUBB4B, 1 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456794copy number variation1nstd102humanUncertain significance GRCh37 chr9: 140,064,816-140,759,229 , GRCh38.p12 chr9: 137,170,364-137,864,777 NELFB, LOC651337, 32 more genes
    nsv4456509copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,766,260-140,186,072 , GRCh38.p12 chr9: 136,871,808-137,291,620 PAXX, CIMIP2A, 40 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4383485copy number variation1nstd173human GRCh37 chr9: 139,059,275-140,803,861 , GRCh38.p12 chr9: 136,167,429-137,909,409 , LRRC26, 107 more genes
    nsv4367274copy number variation1nstd173human GRCh37 chr9: 139,563,040-140,180,735 , GRCh38.p12 chr9: 136,668,588-137,286,283 , LCN10, 67 more genes
    nsv4191916copy number variation1nstd166human GRCh37.p13 chr9: 140,138,412-140,138,462 , GRCh38.p12 chr9: 137,243,960-137,244,010 CIMIP2A, TUBB4B
    nsv4177476copy number variation1nstd166human GRCh37.p13 chr9: 140,128,500-140,137,500 , GRCh38.p12 chr9: 137,234,048-137,243,048 CIMIP2A, TUBB4B, 1 more genes
    nsv4173572copy number variation1nstd166human GRCh37.p13 chr9: 140,036,219-140,618,497 , GRCh38.p12 chr9: 137,141,767-137,724,045 DPH7, ENTPD8, 32 more genes
    nsv3966507copy number variation1nstd168human GRCh38 chr9: 137,241,303-137,366,224 , GRCh37.p13 chr9: 140,135,755-140,260,676 TUBB4B, NELFB, 6 more genes
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