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Items: 1 to 20 of 112

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5944508copy number variation1nstd209human GRCh38 chr19: 12,136,853-12,137,262 , GRCh37.p13 chr19: 12,247,668-12,248,077 , ZNF20, 1 more genes
    nsv5596705copy number variation1nstd207human GRCh38 chr19: 12,132,667-12,132,747 , GRCh37.p13 chr19: 12,243,482-12,243,562 , ZNF20, 1 more genes
    nsv5514002copy number variation1nstd206human GRCh38 chr19: 12,136,853-12,137,273 , GRCh37.p13 chr19: 12,247,668-12,248,088 , ZNF20, 1 more genes
    nsv5359492translocation1nstd200human GRCh38 chr19: 12,136,852-12,136,852 , GRCh38 chr19: 12,137,273-12,137,273 , GRCh37.p13 chr19: 12,248,088-12,248,088 , GRCh37.p13 chr19: 12,247,667-12,247,667 , ZNF20, 1 more genes
    nsv5341363translocation1nstd200human GRCh37 chr19: 12,247,668-12,247,668 , GRCh37 chr19: 12,248,088-12,248,088 , GRCh38.p12 chr19: 12,137,273-12,137,273 , GRCh38.p12 chr19: 12,136,853-12,136,853 , ZNF20, 1 more genes
    nsv5326880copy number variation1nstd204human GRCh37.p13 chr19: 12,247,642-12,248,111 , GRCh38.p13 chr19: 12,136,827-12,137,296 , ZNF20, 1 more genes
    nsv5175066mobile element insertion1nstd203human GRCh38 chr19: 12,131,276-12,131,292 , GRCh37.p13 chr19: 12,242,091-12,242,107 , ZNF20, 1 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5011758copy number variation1nstd200human GRCh38 chr19: 12,121,083-12,135,396 , GRCh37.p13 chr19: 12,231,898-12,246,211 , ZNF20, 1 more genes
    nsv5011755copy number variation1nstd200human GRCh38 chr19: 12,107,341-12,129,615 , GRCh37.p13 chr19: 12,218,156-12,240,430 , ZNF20, 2 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
    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
    nsv4370574copy number variation1nstd173human GRCh37 chr19: 12,247,752-12,433,282 , GRCh38.p12 chr19: 12,136,937-12,322,468 , ZNF20, 10 more genes
    nsv4268778copy number variation1nstd166human GRCh37.p13 chr19: 12,247,668-12,248,117 , GRCh38.p12 chr19: 12,136,853-12,137,302 , ZNF625-ZNF20, 1 more genes
    nsv4259609copy number variation1nstd166human GRCh37.p13 chr19: 12,241,000-12,246,000 , GRCh38.p12 chr19: 12,130,185-12,135,185 , ZNF625-ZNF20, 1 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
    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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