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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3912194copy number variation1nstd102humanLikely benign NCBI36 chr9: 5,342,284-5,416,040 , GRCh37 chr9: 5,352,284-5,426,040 , GRCh38 chr9: 5,352,284-5,426,040 PLGRKT, RNF152P1
    nsv3901590copy number variation1nstd102humanBenign GRCh37 chr9: 5,381,870-5,523,773 , GRCh38.p12 chr9: 5,381,870-5,523,773 PLGRKT, PDCD1LG2, 2 more genes
    nsv3920950copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281 PLGRKT, RPL4P5, 193 more genes
    nsv3910019copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803 PLGRKT, LOC107987049, 191 more genes
    nsv5381767copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814 PLGRKT, ACTG1P14, 191 more genes
    nsv4768366copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359 PLGRKT, DOCK8-AS1, 186 more genes
    nsv3910119copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357 PLGRKT, RNA5SP279, 186 more genes
    nsv3917303copy number variation1nstd102humanPathogenic GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357 PLGRKT, DMAC1, 185 more genes
    nsv4674929copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412 PLGRKT, LINC02851, 184 more genes
    nsv3905168copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300 PLGRKT, RANBP6, 184 more genes
    nsv3899178copy number variation1nstd102humanPathogenic GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752 PLGRKT, GLIS3, 181 more genes
    nsv3903505copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895 PLGRKT, RPS26P3, 179 more genes
    nsv3923785copy number variation1nstd102humanPathogenic NCBI36 chr9: 194,193-16,887,578 , GRCh37 chr9: 204,193-16,897,578 , GRCh38 chr9: 204,193-16,897,580 PLGRKT, FTH1P12, 176 more genes
    nsv3890932copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-16,856,907 , GRCh38.p12 chr9: 203,861-16,856,909 PLGRKT, ACTG1P14, 176 more genes
    nsv3917732copy number variation1nstd102humanPathogenic GRCh38 chr9: 214,367-16,307,944 , GRCh37 chr9: 214,367-16,307,942 , NCBI36 chr9: 204,367-16,297,942 PLGRKT, RLN1, 173 more genes
    nsv3919683copy number variation1nstd102humanPathogenic GRCh38 chr9: 322,690-16,401,656 , NCBI36 chr9: 312,690-16,391,654 , GRCh37 chr9: 322,690-16,401,654 PLGRKT, DMRT2, 172 more genes
    nsv3918828copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,090-15,260,598 , NCBI36 chr9: 194,090-15,250,598 , GRCh38 chr9: 204,090-15,260,600 PLGRKT, HMGN2P31, 160 more genes
    nsv3902507copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-15,211,277 , GRCh38.p12 chr9: 203,861-15,211,279 PLGRKT, MPDZ, 160 more genes
    nsv6634450copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-15,048,247 , GRCh38.p12 chr9: 203,861-15,048,249 PLGRKT, LOC102724027, 157 more genes
    nsv3904963copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-14,744,606 , GRCh38.p12 chr9: 203,861-14,744,608 PLGRKT, LOC105375947, 151 more genes
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