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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5298909copy number variation1nstd204human GRCh38.p13 chr19: 10,842,201-11,593,800 , GRCh37.p13 chr19: 10,952,877-11,704,615 KANK2, RPL18AP13, 35 more genes
    nsv5295569copy number variation1nstd204human GRCh38.p13 chr19: 11,293,101-11,613,000 , GRCh37.p13 chr19: 11,403,777-11,723,815 ELAVL3, ACP5, 21 more genes
    nsv5293507copy number variation1nstd204human GRCh38.p13 chr19: 11,373,770-11,374,869 , GRCh37.p13 chr19: 11,484,446-11,485,545 SWSAP1
    nsv5293211copy number variation1nstd204human GRCh37.p13 chr19: 11,421,777-11,524,376 , GRCh38.p13 chr19: 11,311,101-11,413,700 EPOR, RAB3D, 6 more genes
    nsv5287330copy number variation1nstd204human GRCh38.p13 chr19: 10,335,601-11,755,400 , GRCh37.p13 chr19: 10,446,277-11,866,215 AP1M2, C19orf38, 64 more genes
    nsv5014520copy number variation1nstd200human GRCh38 chr19: 11,376,145-11,385,723 , GRCh37.p13 chr19: 11,486,821-11,496,399 EPOR, SWSAP1
    nsv4860255copy number variation1nstd200human GRCh37 chr19: 11,486,297-11,487,197 , GRCh38.p12 chr19: 11,375,621-11,376,521 EPOR, SWSAP1
    nsv4729806copy number variation1nstd102humanPathogenic GRCh37 chr19: 10,957,601-11,672,041 , GRCh38.p12 chr19: 10,846,925-11,561,226 DOCK6-AS1, C19orf38, 32 more genes
    nsv4685775copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 SLC44A2, ZNF833P, 114 more genes
    nsv4676222copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,445,773-12,160,664 , GRCh38.p12 chr19: 11,335,097-12,049,849 ECSIT, MIR7974, 41 more genes
    nsv4626825copy number variation2nstd183human GRCh37 chr19: 11,485,189-11,486,204 , GRCh38.p12 chr19: 11,374,513-11,375,528 SWSAP1, EPOR
    nsv4451686copy number variation1nstd102humannot provided GRCh37 chr19: 10,642,984-12,810,067 , GRCh38.p12 chr19: 10,532,308-12,699,253 ODAD3, RNA5SP466, 114 more genes
    nsv4271212copy number variation1nstd166human GRCh37.p13 chr19: 11,486,297-11,487,197 , GRCh38.p12 chr19: 11,375,621-11,376,521 SWSAP1, EPOR
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
    nsv3922999copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,240,071-12,946,266 , GRCh37.p13 chr19: 10,379,071-13,085,266 , GRCh38.p12 chr19: 10,268,395-12,974,452 ZNF433, MIR6794, 155 more genes
    nsv3922964copy number variation1nstd102humanPathogenic GRCh38 chr19: 10,319,474-13,777,860 , NCBI36 chr19: 10,291,150-13,749,674 , GRCh37 chr19: 10,430,150-13,888,674 SWSAP1, LOC105372284, 164 more genes
    nsv3920616copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227 ACP5, GET3, 236 more genes
    nsv3915706copy number variation1nstd102humanUncertain significance GRCh38 chr19: 11,138,895-11,549,951 , NCBI36 chr19: 11,110,571-11,521,766 , GRCh37 chr19: 11,249,571-11,660,766 ELAVL3, ECSIT, 22 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
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