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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112759copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,001-8,472,742 , GRCh38.p12 chr3: 18,324-8,431,056 LOC105376926, LOC107986057, 69 more genes
    nsv5894841copy number variation1nstd209human GRCh38 chr3: 1,880,218-5,919,238 , GRCh37.p13 chr3: 1,921,902-5,960,925 , IL5RA, 37 more genes
    nsv5449368copy number variation1nstd206human GRCh38 chr3: 3,063,914-3,065,157 , GRCh37.p13 chr3: 3,105,598-3,106,841 IL5RA
    nsv5381423copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-5,940,479 , GRCh38.p12 chr3: 32,241-5,898,792 ITPR1-DT, RPSAP32, 54 more genes
    nsv5351355translocation1nstd200human GRCh38 chr3: 3,110,247-3,110,247 , GRCh38 chr3: 3,110,354-3,110,354 , GRCh37.p13 chr3: 3,151,931-3,151,931 , GRCh37.p13 chr3: 3,152,038-3,152,038 IL5RA
    nsv5351354translocation1nstd200human GRCh38 chr3: 3,065,157-3,065,157 , GRCh38 chr3: 3,063,914-3,063,914 , GRCh37.p13 chr3: 3,105,598-3,105,598 , GRCh37.p13 chr3: 3,106,841-3,106,841 IL5RA
    nsv5336037translocation1nstd200human GRCh37 chr3: 3,151,931-3,151,931 , GRCh37 chr3: 3,152,038-3,152,038 , GRCh38.p12 chr3: 3,110,247-3,110,247 , GRCh38.p12 chr3: 3,110,354-3,110,354 IL5RA
    nsv5200318copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 73,914-4,356,052 , GRCh38.p12 chr3: 32,241-4,314,368 IL5RA, SETMAR, 35 more genes
    nsv5200317copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 73,914-4,331,711 , GRCh38.p12 chr3: 32,241-4,290,027 IL5RA, CHL1, 34 more genes
    nsv5065062mobile element insertion1nstd203human GRCh38 chr3: 3,071,576-3,071,576 , GRCh37.p13 chr3: 3,113,260-3,113,260 IL5RA
    nsv4914240copy number variation1nstd200human GRCh38 chr3: 1,881,358-4,897,912 , GRCh37.p13 chr3: 1,923,042-4,939,596 , EGOT, 23 more genes
    nsv4910751copy number variation1nstd200human GRCh38 chr3: 3,104,011-3,110,029 , GRCh37.p13 chr3: 3,145,695-3,151,713 IL5RA
    nsv4910750copy number variation1nstd200human GRCh38 chr3: 3,098,965-3,100,948 , GRCh37.p13 chr3: 3,140,649-3,142,632 IL5RA
    nsv4910749copy number variation1nstd200human GRCh38 chr3: 3,079,065-3,088,299 , GRCh37.p13 chr3: 3,120,749-3,129,983 IL5RA
    nsv4910748copy number variation1nstd200human GRCh38 chr3: 3,058,558-3,089,868 , GRCh37.p13 chr3: 3,100,242-3,131,552 CNTN4-AS1, CNTN4, 1 more genes
    nsv4910701copy number variation1nstd200human GRCh38 chr3: 2,238,834-3,629,650 , GRCh37.p13 chr3: 2,280,518-3,671,334 IL5RA, TRNT1, 6 more genes
    nsv4790372copy number variation1nstd200human GRCh37 chr3: 3,145,695-3,151,713 , GRCh38.p12 chr3: 3,104,011-3,110,029 IL5RA
    nsv4790371copy number variation1nstd200human GRCh37 chr3: 3,105,598-3,106,841 , GRCh38.p12 chr3: 3,063,914-3,065,157 IL5RA
    nsv4790370copy number variation1nstd200human GRCh37 chr3: 3,100,261-3,131,539 , GRCh38.p12 chr3: 3,058,577-3,089,855 CNTN4, IL5RA, 1 more genes
    nsv4680078copy number variation1nstd189human GRCh37.p13 chr3: 3,103,111-3,352,713 , GRCh38.p12 chr3: 3,061,427-3,311,029 IL5RA, TRNT1, 2 more genes
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