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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381193copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,912,954-11,200,309 , GRCh38.p12 chr19: 10,802,278-11,089,633 SMARCA4, RN7SL192P, 10 more genes
    nsv5321778copy number variation1nstd204human GRCh37.p13 chr19: 11,035,706-11,044,926 , GRCh38.p13 chr19: 10,925,030-10,934,250 TIMM29, YIPF2
    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
    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
    nsv5286396copy number variation1nstd204human GRCh38.p13 chr19: 10,925,158-10,929,187 , GRCh37.p13 chr19: 11,035,834-11,039,863 YIPF2, TIMM29
    nsv5285730copy number variation1nstd204human GRCh38.p13 chr19: 10,872,301-10,941,400 , GRCh37.p13 chr19: 10,982,977-11,052,076 TIMM29, CARM1, 1 more genes
    nsv5281589copy number variation1nstd204human GRCh38.p13 chr19: 10,925,001-10,934,300 , GRCh37.p13 chr19: 11,035,677-11,044,976 TIMM29, YIPF2
    nsv4860231copy number variation1nstd200human GRCh37 chr19: 11,035,716-11,044,918 , GRCh38.p12 chr19: 10,925,040-10,934,242 YIPF2, TIMM29
    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
    nsv4676283copy number variation1nstd102humanUncertain significance GRCh37 chr19: 10,632,623-11,135,294 , GRCh38.p12 chr19: 10,521,947-11,024,618 ATG4D, RN7SL192P, 21 more genes
    nsv4628878copy number variation1nstd183human GRCh37 chr19: 11,038,590-11,039,498 , GRCh38.p12 chr19: 10,927,914-10,928,822 TIMM29, YIPF2
    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
    nsv4336796sequence alteration1nstd166human GRCh37.p13 chr19: 11,034,072-11,038,062 , GRCh38.p12 chr19: 10,923,396-10,927,386 CARM1, YIPF2, 1 more genes
    nsv4272188copy number variation1nstd166human GRCh37.p13 chr19: 11,037,160-11,053,286 , GRCh38.p12 chr19: 10,926,484-10,942,610 TIMM29, YIPF2
    nsv4271714copy number variation1nstd166human GRCh37.p13 chr19: 11,038,619-11,058,403 , GRCh38.p12 chr19: 10,927,943-10,947,727 TIMM29, YIPF2
    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
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