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Dilated cardiomyopathy (WES based NGS panel of 81 genes, including CNV analysis)
ABCC9, ACTC1, ACTN2, BAG3, CSRP3, DES, DMD, DSP, EPG5, EYA4, FKTN, HAMP, HCN4, HFE, HFE2, IDH2, KCND3, LDB3, LMNA, MYBPC3, MYH6, MYH7, NEXN, PLN, RAB3GAP2, RBM20, SCN5A, SGCD, SLC40A1, TAZ, TCAP, TFR2, TNNC1, TNNI3, TNNT2, TPM1, TTN, VCL, ANKRD1, CRYAB, G
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Methodology

NGS


Specimen Requirements


Descriptive Volume /
Concentration 1
Container Transport
temperature
Sample
viability (days) 2
DNA ≥ 100 µL [50 ng/µL] Eppendorf Safe-lock Room temp. n/a
Peripheral blood ≥ 3 mL EDTA Room temp. 5
1 When it is not possible to collect the minimum volume for the test, please contact CGC Genetics
2 Maximum shipping time to ensure sample quality

Turnaround Time (Days)

- 60

Specialties

- Cardiology, Rare diseases


CGC Reference

- 5570




Associated Tests


Left ventricular noncompaction (LVNC, NGS panel of 13 genes)
Cardiomyopathy (hypertrophic, dilated , arrhythmogenic right ventricular dysplasia and left ventricular noncompaction) and changes in cardiac conduction (WES based NGS panel of 140 genes, including CNV analysis)
Hypertrophic cardiomyopathy (WES based NGS panel of 68 genes, including CNV analysis)
Arrhythmogenic right ventricular dysplasia (NGS panel of 15 genes)
Limb-girdle muscular dystrophies (NGS panel of 42 genes)