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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938003copy number variation1nstd209human GRCh38 chr19: 11,547,083-11,547,185 , GRCh37.p13 chr19: 11,657,898-11,658,000 CNN1
    nsv5594678copy number variation1nstd207human GRCh38 chr19: 11,547,083-11,547,185 , GRCh37.p13 chr19: 11,657,898-11,658,000 CNN1
    nsv5518636copy number variation1nstd206human GRCh38 chr19: 11,547,088-11,547,186 , GRCh37.p13 chr19: 11,657,903-11,658,001 CNN1
    nsv5515487copy number variation1nstd206human GRCh38 chr19: 11,538,095-11,538,219 , GRCh37.p13 chr19: 11,648,910-11,649,034 CNN1
    nsv5325621copy number variation1nstd204human GRCh38.p13 chr19: 11,548,523-11,548,809 , GRCh37.p13 chr19: 11,659,338-11,659,624 CNN1
    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
    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
    nsv5011700copy number variation1nstd200human GRCh38 chr19: 11,543,613-11,546,234 , GRCh37.p13 chr19: 11,654,428-11,657,049 CNN1
    nsv4860265copy number variation1nstd200human GRCh37 chr19: 11,659,347-11,659,616 , GRCh38.p12 chr19: 11,548,532-11,548,801 CNN1
    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
    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
    nsv4263483copy number variation1nstd166human GRCh37.p13 chr19: 11,657,903-11,658,001 , GRCh38.p12 chr19: 11,547,088-11,547,186 CNN1
    nsv3960925copy number variation1nstd168human GRCh38 chr19: 11,513,686-11,558,109 , GRCh37.p13 chr19: 11,624,501-11,668,924 CNN1, ECSIT, 4 more genes
    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
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