GeneSeq: Cardio - Familial Cardiomyopathy Panel
Clinical Genetic Test
offered by
GTR Test Accession: Help GTR000604229.2
Last updated in GTR: 2023-09-24
Last annual review date for the lab: 2024-01-10 LinkOut
At a Glance
Congenital disorder of glycosylation; Alstrom syndrome; Apolipoprotein A-I deficiency; ...
ABCC9 (12p12.1), ACTC1 (15q14), ACTN2 (1q43), ALMS1 (2p13.1), ALPK3 (15q25.3), ...
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
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Ordering Information
Offered by: Help
Integrated Genetics Westborough
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Informed consent required: Help
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Pre-test genetic counseling required: Help
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Post-test genetic counseling required: Help
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Conditions Help
Total conditions: 17
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 67
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Total methods: 1
Method Category Help
Test method Help
Instrument *
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
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Technical Information
Test Comments: Help
Next-generation sequencing to identify genetic variants, including small nucleotide variants (SNVs), insertions and deletions. Copy number variants (CNVs) are assessed and reported for the DMD gene only. TTN excludes exons 154 and 155.
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Analytical sensitivity at 30X coverage is estimated to be >99% for single nucleotide variants, >99% for insertions/deletions less than six base pairs and >96% for insertions/deletions between six and forty-five base pairs.
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
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Regulatory Approval
FDA Review: Help
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Additional Information

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