LabCorp and its Specialty Testing Group, a fully integrated portfolio of specialty and esoteric testing laboratories.

Reveal® SNP microarray

Reveal has application for pediatric (peripheral blood and buccal swab), prenatal (amniocytes or chorionic villi) and product of conception (POC) sample types.

Oftentimes, a patient’s or fetus’ phenotype does not fit a specific syndrome, and it is in these cases that patients benefit most from microarray analysis.

Reveal will identify the abnormalities currently detected by routine cytogenetics (with the exception of balanced chromosome translocations). It will also identify other abnormalities that are undetectable by routine cytogenetics. And with more than 190,000 arrays analyzed, Integrated Genetics has an extensive database of abnormalities providing an exceptional reference to support interpretation.

Reveal

Reveal SNP microarray - Prenatal: detects genomic imbalance related to congenital anomalies, ultrasound abnormalities, miscarriage, and stillbirth. Can also detect copy neutral changes, such as uniparental disomy (UPD) and consanguinity, both of which are associated with increased risk for autosomal recessive conditions.

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Reveal SNP microarray - Pediatric: enhances the detection of chromosome abnormalities. Clinical Indications: Individuals with non-syndromic congenital anomalies, dysmorphic features, developmental delay, intellectual disability, and/or autism spectrum disorders (ASD).

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Reveal SNP microarray - POC: detects chromosomal imbalances related to fetal loss. Can be performed directly on POC tissue without having to grow cells, optimizing success rate and turnaround time.

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Reveal SNP microarray and abbreviated chromosome analysis (amniotic fluid): detects genomic imbalance related to congenital anomalies, ultrasound abnormalities, miscarriage and stillbirth. Can also detect copy neutral changes such as UPD and consanguinity, both of which are associated with increased risk for autosomal recessive conditions.

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Reveal SNP microarray and abbreviated chromosome analysis (CVS): detects genomic imbalance related to congenital anomalies, ultrasound abnormalities, miscarriage and stillbirth. Can also detect copy neutral changes such as UPD and consanguinity, both of which are associated with increased risk for autosomal recessive conditions.

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Other testing options

In addition to diagnostic testing, we also offer: serum screening and noninvasive prenatal testing (NIPT, sometimes called NIPS or cell-free DNA), including the pioneering whole-genome NIPTcarrier screening, from comprehensive to single-gene; and hereditary cancer screening.

Do you have patients who have not had a test and have questions about costs or coverage? Send them to our estimator.

Do you have patients who have already had a test performed and are wondering when their results will be in? We can help.

Patients with questions about their test results who need schedule an appointment with a counselor can do so online.