Select a pre-curated test, combine multiple tests, or customize your own test for each patient. Invitae's pricing is per "(external) clinical area(clinical area)":/clinical-areas/ for initial order and "(external) re-requisition(Re-requisition)":/re-requisition/. 

All the tests on this page and in "(external) Neurology":/physician/category/CAT000009/ fall into a single clinical area. If your order contains tests from multiple clinical areas, you will need to send in two sample tubes and your order will represent two billable events. Your test results will be delivered as two reports. Please contact Client Services with any questions. 

Cardiology

ADAMTS10

ACTA2

TGFB2

SLC2A10

FBN1

TGFBR1

SMAD2

MYH11

COL5A2

TGFBR2

TGFB3

SMAD3

PLOD1

PRKG1

COL3A1

FOXE3

MED12

SMAD4

FLNA

COL5A1

NOTCH1

MYLK

FBN2

MFAP5

EFEMP2

Analyzes genes which cause aortopathy, presenting as isolated thoracic aortic aneurysms and dissections (TAAD) or as a syndrome.

Invitae Aortopathy Comprehensive Panel

SMAD6

PLOD3

HCN4

MAT2A

LTBP3

ARIH1

Add-on Preliminary-evidence Genes for Aortopathy

TNNT2

TRDN

ABCC9

CALM3

PKP2

GJA5

CDH2

FLNC

TRPM4

KCNE1

TNNI3

CACNA1C

CALM1

PRKAG2

DSG2

LMNA

KCNH2

CASQ2

GATA4

GATA5

KCNJ2

DSC2

CALM2

KCNQ1

PPA2

BAG3

CACNA1D

RBM20

ACTN2

SCN5A

TMEM43

RYR2

MYL4

NKX2-5

Analyzes genes that are associated with arrhythmia and arrhythmogenic cardiomyopathy, including long QT syndrome (LQTS), short QT syndrome (SQTS), Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia (CPVT), and arrhythmogenic right ventricular cardiomyopathy (ARVC).

Invitae Arrhythmia Comprehensive Panel

CACNB2

LDB3

SCN2B

RANGRF

SCN10A

GATA6

ANK2

GPD1L

CAV3

ANKRD1

CACNA2D1

CTNNA3

SCN1B

SCN4B

NPPA

KCNJ5

AKAP9

SLMAP

SCN3B

SNTA1

KCND3

KCNK3

KCNE3

KCNE5

KCNA5

KCNJ8

PDLIM3

KCNE2

Add-on Preliminary-evidence Genes for Arrhythmia

KCNQ2

SCN9A

PCDH19

PRRT2

DEPDC5

KCNQ3

SLC2A1

KCNA1

KCNT1

SCN8A

SCN1A

Add-on Sudden Unexpected Death in Epilepsy (SUDEP) Genes

SGCD

SPRED1

EYA4

FKTN

LZTR1

MYL3

RAF1

PPP1CB

MRAS

CRYAB

MYLK3

MAP2K2

PPCS

FKRP

ALMS1

PTPN11

MYH7

SDHA

RIT1

SOS1

TNNC1

CPT2

KRAS

ALPK3

MYBPC3

SOS2

TPM1

DNAJC19

MAP2K1

MTO1

ACADVL

TNNI3K

TMEM70

MYL2

CSRP3

PCCB

PCCA

TCAP

SHOC2

SLC22A5

LAMP2

FHL1

NRAS

ACTC1

BRAF

DOLK

ELAC2

RASA1

HRAS

TBX20

Analyzes genes that are associated with primary arrhythmia and/or cardiomyopathy, as well as syndromic causes of cardiomyopathy.

Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel

MYPN

MAP3K8

TMPO

MYOM1

RASA2

LAMA4

RRAS

NEBL

MYLK2

GATAD1

CALR3

MYH6

DTNA

A2ML1

CHRM2

JPH2

TXNRD2

NEXN

CTF1

KIF20A

FHL2

KLF10

LRRC10

PRDM16

PLEKHM2

MYOZ2

HAND1

Add-on Preliminary-evidence Genes for Arrhythmia and Cardiomyopathy

Analyzes genes that are associated with arrhythmogenic cardiomyopathy, including arrhythmogenic right ventricular cardiomyopathy (ARVC) and arrhythmogenic forms of dilated cardiomyopathy (DCM) and hypertrophic cardiomyopathy (HCM).

Invitae Arrhythmogenic Cardiomyopathy Panel

Add-on Preliminary-evidence Genes for Arrhythmogenic Cardiomyopathy

Genetic testing for up to 20 genes that cause Brugada syndrome, an arrhythmia that can cause fainting, seizure-like episodes, or cardiac arrest.

Invitae Brugada Syndrome Test

Add-on Preliminary-evidence Genes for Brugada Syndrome

Analyzes genes that are associated with cardiomyopathy, a broad group of conditions characterized by an enlarged, stiff or weakened heart muscle.

Invitae Cardiomyopathy Comprehensive Panel