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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937731copy number variation1nstd209human GRCh38 chr19: 12,183,985-12,184,278 , GRCh37.p13 chr19: 12,294,800-12,295,093 ZNF136
    nsv5936169copy number variation1nstd209human GRCh38 chr19: 12,182,097-12,182,230 , GRCh37.p13 chr19: 12,292,912-12,293,045 ZNF136
    nsv5657458insertion1nstd207human GRCh38 chr19: 12,170,084-12,170,084 , GRCh37.p13 chr19: 12,280,899-12,280,899 ZNF136
    nsv5601584copy number variation1nstd207human GRCh38 chr19: 12,170,037-12,170,170 , GRCh37.p13 chr19: 12,280,852-12,280,985 ZNF136
    nsv5531102copy number variation1nstd206human GRCh38 chr19: 12,182,097-12,182,233 , GRCh37.p13 chr19: 12,292,912-12,293,048 ZNF136
    nsv5524743copy number variation1nstd206human GRCh38 chr19: 12,170,693-12,170,834 , GRCh37.p13 chr19: 12,281,508-12,281,649 ZNF136
    nsv5325469copy number variation1nstd204human GRCh38.p13 chr19: 12,168,942-12,170,184 , GRCh37.p13 chr19: 12,279,757-12,280,999 ZNF136
    nsv5325326copy number variation1nstd204human GRCh38.p13 chr19: 12,170,039-12,171,195 , GRCh37.p13 chr19: 12,280,854-12,282,010 ZNF136
    nsv5285263copy number variation1nstd204human GRCh38.p13 chr19: 12,168,901-12,170,200 , GRCh37.p13 chr19: 12,279,716-12,281,015 ZNF136
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5011766copy number variation1nstd200human GRCh38 chr19: 12,180,714-12,180,779 , GRCh37.p13 chr19: 12,291,529-12,291,594 ZNF136
    nsv5011765copy number variation1nstd200human GRCh38 chr19: 12,178,988-12,180,192 , GRCh37.p13 chr19: 12,289,803-12,291,007 ZNF136
    nsv5011764copy number variation1nstd200human GRCh38 chr19: 12,169,976-12,180,058 , GRCh37.p13 chr19: 12,280,791-12,290,873 ZNF136
    nsv5011763copy number variation1nstd200human GRCh38 chr19: 12,169,934-12,170,987 , GRCh37.p13 chr19: 12,280,749-12,281,802 ZNF136
    nsv5011762copy number variation1nstd200human GRCh38 chr19: 12,169,744-12,170,931 , GRCh37.p13 chr19: 12,280,559-12,281,746 ZNF136
    nsv5011761copy number variation1nstd200human GRCh38 chr19: 12,168,950-12,170,176 , GRCh37.p13 chr19: 12,279,765-12,280,991 ZNF136
    nsv5011760copy number variation1nstd200human GRCh38 chr19: 12,163,351-12,163,410 , GRCh37.p13 chr19: 12,274,166-12,274,225 ZNF136
    nsv4860303copy number variation1nstd200human GRCh37 chr19: 12,291,529-12,291,594 , GRCh38.p12 chr19: 12,180,714-12,180,779 ZNF136
    nsv4860302copy number variation1nstd200human GRCh37 chr19: 12,289,803-12,291,007 , GRCh38.p12 chr19: 12,178,988-12,180,192 ZNF136
    nsv4860301copy number variation1nstd200human GRCh37 chr19: 12,280,819-12,290,873 , GRCh38.p12 chr19: 12,170,004-12,180,058 ZNF136
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