Test Description

This test is designed to give you a full body of information on any chromosomal abnormalities, Copy Number Variants (CNVs), Loss of Heterozygosity (LOH), and Single Nucleotide Polymorphisms (SNPs) you may have or may have inherited from your parents.

We screen your whole chromosomes against multiple genes to reveal any hidden abnormalities known or unknown to you.

It also confirms and monitors any pathologist’s findings.

We screen for the following conditions

*Hematologic (leukemia, lymphoma, MDS (myelodysplastic syndrome), or MPN (myeloproliferative neoplasm)

*Solid tumors (breast, skin, lung, esophagus, colon, intestine, brain…)

*Somatic Cancers (breast, skin, lung, esophagus, colon, intestine, brain…)

Benefits of this test

*Identifying genetic disorders

*Allowing for early treatment and management

*Enabling informed decisions about healthcare and family planning

*Guide treatment decisions a provide a sense of relief for uncertainty

Who can order this test

Healthcare providers

Test order

*From your healthcare provider’s office.

*If the test is ordered by your healthcare provider’s office, we will mail the collection kits and instructions to their office.

Results

We follow the Clinical Interpretation of Variants in Cancer (CIVIC) and Genomics (ACMG) guidelines for reporting.

Any finds will be interpreted as followed:

Pathogenic

Likely pathogenic

VUS (Variant of unknown significance)

Benign

Likely benign

However, it is important to note that genetic testing has limitations and may not be able to detect all genetic defects. The genetic results do not necessarily mean that you will develop a condition. It identifies the genes or mutations that increase your risk of developing a particular condition.