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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5295678copy number variation1nstd204human GRCh38.p13 chr19: 12,445,401-12,989,100 , GRCh37.p13 chr19: 12,556,215-13,099,914 GCDH, RPL10P16, 46 more genes
    nsv5291223copy number variation1nstd204human GRCh38.p13 chr19: 12,782,101-12,795,000 , GRCh37.p13 chr19: 12,892,915-12,905,814 PRDX2, JUNB, 1 more genes
    nsv5282549copy number variation1nstd204human GRCh38.p13 chr19: 12,584,101-13,543,500 , GRCh37.p13 chr19: 12,694,915-13,654,314 , NFIX, 50 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4645790copy number variation1nstd186human GRCh37 chr19: 12,898,000-12,905,050 , GRCh38.p12 chr19: 12,787,186-12,794,236 MIR5684, JUNB
    nsv4630529copy number variation2nstd183human GRCh37 chr19: 12,735,946-13,097,039 , GRCh38.p12 chr19: 12,625,132-12,986,225 MAST1, SNORD41, 35 more genes
    nsv4629336copy number variation1nstd183human GRCh37 chr19: 12,295,610-12,947,938 , GRCh38.p12 chr19: 12,184,795-12,837,124 , DHPS, 44 more genes
    nsv4626399copy number variation1nstd183human GRCh37 chr19: 12,902,452-12,904,133 , GRCh38.p12 chr19: 12,791,638-12,793,319 JUNB
    nsv4457524copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,354,642-13,424,014 , GRCh38.p12 chr19: 12,243,827-13,313,200 BEST2, TRMT1, 64 more genes
    nsv4270972copy number variation1nstd166human GRCh37.p13 chr19: 12,898,000-12,905,050 , GRCh38.p12 chr19: 12,787,186-12,794,236 JUNB, MIR5684
    nsv4266095copy number variation1nstd166human GRCh37.p13 chr19: 12,900,461-12,900,559 , GRCh38.p12 chr19: 12,789,647-12,789,745 JUNB
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    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
    nsv3919036copy number variation1nstd102humanPathogenic GRCh37 chr19: 11,628,640-13,336,101 , NCBI36 chr19: 11,489,640-13,197,101 , GRCh38 chr19: 11,517,825-13,225,287 ZNF763, RTBDN, 105 more genes
    nsv3915094copy number variation1nstd102humanPathogenic GRCh38 chr19: 12,132,052-14,751,798 , NCBI36 chr19: 12,103,867-14,723,610 , GRCh37 chr19: 12,242,867-14,862,610 RN7SL619P, ZNF625-ZNF20, 123 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
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