Clincally Validated Genetic Tests

We provide genomic products that harness the power of cutting edge science and technology to deliver you the most accurate results.

HAE panel sequencing (77 genes) – peripheral blood

Sequencing and analysis of genes associated with hereditary angioedema.

SERPING1 (C1INH) and F12

Exon level duplication/deletion analysis

Comprehensive Immunodeficiency panel (470 genes) – peripheral blood

Sequencing and analysis of genes associated with inherited disorders of the immune system.

KIT D816V

KIT D816V mutation in peripheral blood has been proposed to be included in the diagnostic work-up of systemic mastocytosis. This is a hotspot test for this mutation only.

Alpha-tryptasemia copy number variation test

Exome Sequencing

Virant DX exome sequencing generates sequencing reads that docus on the protien-coding region of the genome. This comprehensive genetic test can identify changes in a patients DNS that are causative or related to media and family histories of disease. Exome sequencing is intended for use in conjunction with the clinical presentation and other markers of disease progression for the management of patients with rate genetic disorders.