Targeted Variants

Brain Tumor : 1p/19q Co-Deletion Analysis

Brain Tumor : 1p/19q Co-Deletion Analysis

Brain Tumor : CDKN2A/B Deletion Analysis

Brain Tumor : CDKN2A/B Deletion Analysis

Brain Tumor : EGFR Amplification Analysis

Brain Tumor : EGFR Amplification Analysis

Brain Tumor : IDH1 R132H Variant Analysis

Brain Tumor : IDH1 R132H Variant Analysis

Brain Tumor : NEK1 Deletion Analysis

Brain Tumor : NEK1 Deletion Analysis

Brain Tumor : NF1 Deletion Analysis

Brain Tumor : NF1 Deletion Analysis

Brain Tumor : PTEN Deletion Analysis

Brain Tumor : PTEN Deletion Analysis

Brain Tumor : TP53 Deletion Analysis

Brain Tumor : TP53 Deletion Analysis

Colorectal Cancer : KRAS Variant Analysis

Colorectal Cancer : KRAS Variant Analysis

Colorectal Cancer : NRAS Variant Analysis

Colorectal Cancer : NRAS Variant Analysis

Lung Adenocarcinoma : BRAF Mutation analysis (V600E)

Lung Adenocarcinoma : BRAF Mutation analysis (V600E)

Lung Adenocarcinoma : EGFR Amplification and Mutation Analysis

Lung Adenocarcinoma : EGFR Amplification and Mutation Analysis

Lung Adenocarcinoma : EGFR Mutation Analysis

Lung Adenocarcinoma : EGFR Mutation Analysis

Lung Adenocarcinoma : PTEN Mutation Analysis

Lung Adenocarcinoma : PTEN Mutation Analysis

Melanoma : BRAF Mutation Analysis (V600E & V600K)

Melanoma : BRAF Mutation Analysis (V600E & V600K)

Meet Reggie Roper

Meet Reggie Roper

Reggie has been part of the GGC family for over 18 years. He has short stature, webbing of his hands, pulmonary stenosis, seizures and hydrocephalus along with developmental delay. He carried an initial diagnosis of cardiofaciocutaneous (CFC) syndrome; however, as genetic testing advanced, GGC made the diagnosis of Noonan-like syndrome with loose anagen hair by identifying a mutation in the SHOC2 gene. He is also an active participant in the Greenwood Community Theatre's Penguin Project. "GGC is...

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