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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5600695copy number variation1nstd207human GRCh38 chr9: 113,406,669-113,406,969 , GRCh37.p13 chr9: 116,168,949-116,169,249 POLE3
    nsv5316096copy number variation1nstd204human GRCh38.p13 chr9: 113,406,663-113,407,024 , GRCh37.p13 chr9: 116,168,943-116,169,304 POLE3
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983267copy number variation1nstd200human GRCh38 chr9: 113,408,662-113,408,766 , GRCh37.p13 chr9: 116,170,942-116,171,046 POLE3, C9orf43
    nsv4839245copy number variation1nstd200human GRCh37 chr9: 116,167,516-116,168,299 , GRCh38.p12 chr9: 113,405,236-113,406,019 POLE3
    nsv4603895copy number variation1nstd183human GRCh37 chr9: 116,171,837-116,173,357 , GRCh38.p12 chr9: 113,409,557-113,411,077 C9orf43, POLE3
    nsv4599438copy number variation1nstd183human GRCh37 chr9: 116,171,981-116,175,684 , GRCh38.p12 chr9: 113,409,701-113,413,404 POLE3, C9orf43
    nsv4457284copy number variation1nstd102humanUncertain significance GRCh37 chr9: 116,034,704-116,199,658 , GRCh38.p12 chr9: 113,272,424-113,437,378 RNF183, C9orf43, 7 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
    nsv4456379copy number variation1nstd102humanUncertain significance GRCh37 chr9: 113,982,711-117,443,628 , GRCh38.p12 chr9: 111,220,431-114,681,348 MIR4668, LOC100418705, 74 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
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv4191106copy number variation1nstd166human GRCh37.p13 chr9: 116,157,180-116,169,221 , GRCh38.p12 chr9: 113,394,900-113,406,941 ALAD, POLE3
    nsv4189193copy number variation1nstd166human GRCh37.p13 chr9: 116,039,902-116,207,768 , GRCh38.p12 chr9: 113,277,622-113,445,488 ALAD, RGS3, 7 more genes
    nsv3922685copy number variation1nstd102humanPathogenic GRCh38 chr9: 88,522,292-113,687,796 , NCBI36 chr9: 90,327,027-115,489,897 , GRCh37 chr9: 91,137,207-116,450,076 MUSK, LOC105376176, 464 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
    nsv3922633copy number variation2nstd102humanPathogenic GRCh38 chr9: 99,138,048-115,011,033 , NCBI36 chr9: 100,940,151-116,813,133 , GRCh37 chr9: 101,900,330-117,773,312 RAD23B, RNU6-432P, 262 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
    nsv3920713copy number variation1nstd102humanPathogenic NCBI36 chr9: 193,862-140,140,210 , GRCh38 chr9: 203,862-138,125,937 , GRCh37 chr9: 203,862-141,020,389 ABHD17B, LOC100533707, 2167 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 LOC107987031, LOC105376234, 2169 more genes
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