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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
    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
    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
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 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
    nsv4182226copy number variation1nstd166human GRCh37.p13 chr9: 139,880,503-139,894,001 , GRCh38.p12 chr9: 136,986,051-136,999,549 CLIC3, LCNL1, 1 more genes
    nsv3924922copy number variation1nstd102humanPathogenic GRCh38 chr9: 133,504,071-138,159,073 , NCBI36 chr9: 135,314,179-140,173,346 , GRCh37 chr9: 136,324,358-141,053,525 SETP5, NRARP, 178 more genes
    nsv3924554copy number variation2nstd102humanPathogenic GRCh38 chr9: 136,323,974-138,014,606 , NCBI36 chr9: 138,338,249-140,028,879 , GRCh37 chr9: 139,218,428-140,909,058 NRARP, MAN1B1-DT, 104 more genes
    nsv3922926copy number variation1nstd102humanPathogenic NCBI36 chr9: 137,483,683-139,628,011 , GRCh37 chr9: 138,343,862-140,508,190 , GRCh38 chr9: 135,452,016-137,613,738 SSNA1, LOC107987140, 126 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
    nsv3921598copy number variation1nstd102humanPathogenic GRCh38 chr9: 203,861-138,125,937 , NCBI36 chr9: 193,861-140,140,210 , GRCh37 chr9: 203,861-141,020,389 PGAP4, ECPAS, 2167 more genes
    nsv3920829copy number variation1nstd102humanPathogenic GRCh38 chr9: 121,112,395-138,075,224 , GRCh37 chr9: 123,874,673-140,969,676 , NCBI36 chr9: 122,914,494-140,089,497 LOC101928786, NRON, 495 more genes
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