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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947001copy number variation1nstd209human GRCh38 chr19: 48,323,295-48,324,508 , GRCh37.p13 chr19: 48,826,552-48,827,765 EMP3
    nsv5880594copy number variation1nstd209human GRCh38 chr19: 48,323,105-48,324,562 , GRCh37.p13 chr19: 48,826,362-48,827,819 EMP3
    nsv5667352inversion1nstd207human GRCh38 chr19: 47,959,661-50,091,195 , GRCh37.p13 chr19: 48,462,918-50,594,452 , AP2A1, 145 more genes
    nsv5523833copy number variation1nstd206human GRCh38 chr19: 48,323,296-48,324,509 , GRCh37.p13 chr19: 48,826,553-48,827,766 EMP3
    nsv5359876translocation1nstd200human GRCh38 chr19: 48,324,509-48,324,509 , GRCh38 chr19: 48,323,296-48,323,296 , GRCh37.p13 chr19: 48,827,766-48,827,766 , GRCh37.p13 chr19: 48,826,553-48,826,553 EMP3
    nsv5333263translocation1nstd200human GRCh37 chr19: 48,827,766-48,827,766 , GRCh37 chr19: 48,826,553-48,826,553 , GRCh38.p12 chr19: 48,324,509-48,324,509 , GRCh38.p12 chr19: 48,323,296-48,323,296 EMP3
    nsv5020900copy number variation1nstd200human GRCh38 chr19: 48,324,805-48,325,706 , GRCh37.p13 chr19: 48,828,062-48,828,963 EMP3
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
    nsv4672267copy number variation1nstd186human GRCh37 chr19: 48,826,499-48,827,735 , GRCh38.p12 chr19: 48,323,242-48,324,478 EMP3
    nsv4634188copy number variation1nstd183human GRCh37 chr19: 48,826,499-48,827,735 , GRCh38.p12 chr19: 48,323,242-48,324,478 EMP3
    nsv4457853copy number variation1nstd102humanUncertain significance GRCh37 chr19: 48,119,589-49,595,956 , GRCh38.p12 chr19: 47,616,332-49,092,699 DHDH, GRIN2D, 94 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4420917copy number variation1nstd174human GRCh37 chr19: 48,826,481-48,827,768 , GRCh38.p12 chr19: 48,323,224-48,324,511 EMP3
    nsv4383630copy number variation1nstd173human GRCh37 chr19: 48,688,159-48,858,455 , GRCh38.p12 chr19: 48,184,902-48,355,198 EMP3, CARD8, 7 more genes
    nsv4376838copy number variation1nstd173human GRCh37 chr19: 48,462,617-51,107,899 , GRCh38.p12 chr19: 47,959,360-50,604,642 , LIN7B, 173 more genes
    nsv4321864inversion1nstd166human GRCh37.p13 chr19: 46,657,897-51,634,775 , GRCh38.p12 chr19: 46,154,640-51,131,518 , C5AR1, 288 more genes
    nsv4261120copy number variation1nstd166human GRCh37.p13 chr19: 48,826,553-48,827,766 , GRCh38.p12 chr19: 48,323,296-48,324,509 EMP3
    nsv4259209copy number variation1nstd166human GRCh37.p13 chr19: 48,765,333-48,828,053 , GRCh38.p12 chr19: 48,262,076-48,324,796 ZNF114-AS1, ZNF114, 2 more genes
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