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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940838copy number variation1nstd209human GRCh38 chr19: 10,869,944-10,870,956 , GRCh37.p13 chr19: 10,980,620-10,981,632 CARM1, C19orf38
    nsv5938748copy number variation1nstd209human GRCh38 chr19: 10,894,714-10,899,578 , GRCh37.p13 chr19: 11,005,390-11,010,254 CARM1
    nsv5930660copy number variation1nstd209human GRCh38 chr19: 10,880,831-10,880,960 , GRCh37.p13 chr19: 10,991,507-10,991,636 CARM1
    nsv5884383copy number variation1nstd209human GRCh38 chr19: 10,894,716-10,899,463 , GRCh37.p13 chr19: 11,005,392-11,010,139 CARM1
    nsv5537435insertion1nstd206human GRCh38 chr19: 10,901,933-10,901,948 , GRCh37.p13 chr19: 11,012,609-11,012,624 CARM1
    nsv5527915copy number variation1nstd206human GRCh38 chr19: 10,880,832-10,880,961 , GRCh37.p13 chr19: 10,991,508-10,991,637 CARM1
    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
    nsv5359479translocation1nstd200human GRCh38 chr19: 10,880,832-10,880,832 , GRCh38 chr19: 10,880,961-10,880,961 , GRCh37.p13 chr19: 10,991,508-10,991,508 , GRCh37.p13 chr19: 10,991,637-10,991,637 CARM1
    nsv5324996copy number variation1nstd204human GRCh38.p13 chr19: 10,880,826-10,880,966 , GRCh37.p13 chr19: 10,991,502-10,991,642 CARM1
    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
    nsv5297616copy number variation1nstd204human GRCh38.p13 chr19: 10,882,301-10,886,800 , GRCh37.p13 chr19: 10,992,977-10,997,476 CARM1
    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
    nsv5286584copy number variation1nstd204human GRCh37.p13 chr19: 10,844,077-10,981,976 , GRCh38.p13 chr19: 10,733,401-10,871,300 DNM2, CARM1, 5 more genes
    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
    nsv5173237mobile element insertion1nstd203human GRCh38 chr19: 10,906,924-10,906,928 , GRCh37.p13 chr19: 11,017,600-11,017,604 CARM1
    nsv5169884mobile element insertion1nstd203human GRCh38 chr19: 10,907,241-10,907,258 , GRCh37.p13 chr19: 11,017,917-11,017,934 CARM1
    nsv5166122mobile element insertion1nstd203human GRCh38 chr19: 10,909,693-10,909,742 , GRCh37.p13 chr19: 11,020,369-11,020,418 CARM1
    nsv5164526mobile element insertion1nstd203human GRCh38 chr19: 10,873,441-10,873,453 , GRCh37.p13 chr19: 10,984,117-10,984,129 CARM1
    nsv5011638copy number variation1nstd200human GRCh38 chr19: 10,886,646-10,900,165 , GRCh37.p13 chr19: 10,997,322-11,010,841 CARM1
    nsv4860230copy number variation1nstd200human GRCh37 chr19: 11,017,278-11,017,628 , GRCh38.p12 chr19: 10,906,602-10,906,952 CARM1
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