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/. 

The tests and genes on this page are organized into clinical areas. 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.

Nephrology

CD151

COL4A4

COL4A6

COL4A3

MYH9

COL4A5

Genetic testing for genes associated with Alport syndrome which is generally characterized by renal disease and deafness with possible ocular findings including anterior lenticonus and cataract.

Invitae Alport Syndrome Panel

ADAMTS13

DGKE

INF2

CD55

CD46

CD59

THBD

MMACHC

The Invitae Atypical Hemolytic Uremic Syndrome and Thrombotic Microangiopathies Panel analyzes genes which are associated with thrombotic microangiopathies, including atypical hemolytic uremic syndrome and thrombotic thrombocytopenic purpura. These conditions are characterized by hemolytic anemia, thrombocytopenia, and kidney damage which may progress to kidney failure.

Invitae Atypical Hemolytic Uremic Syndrome and Thrombotic Microangiopathies Panel

BBS12

LZTFL1

KIF7

BBS9

BBIP1

BBS4

C8orf37

CEP164

BBS10

FBN3

BBS7

BBS1

SDCCAG8

CEP290

WDPCP

BBS2

ARL6

IFT172

SCLT1

TRIM32

CEP19

IFT27

TRAPPC3

IFT74

MKS1

TTC8

BBS5

MKKS

The Invitae Bardet-Biedl Syndrome  Panel analyzes genes that are associated with Bardet-Biedl Syndrome (BBS), which is characterized by truncal obesity, cognitive impairment rod-cone dystrophy, and renal abnormalities. These genes were selected based on the available evidence to date to provide a broad analysis for BBS.

Invitae Bardet-Biedl Syndrome Panel

ARMC4

B9D2

DNAAF3

RSPH4A

DCDC2

DNAH8

CCNO

CRB2

INPP5E

CEP83

ADAMTS9

TMEM138

TMEM237

DNAI2

LRRCC1

PMM2

DNAAF5

B9D1

HNF1B

CSPP1

ARL13B

DNAAF4

CCDC151

EXOC8

WDR19

CC2D2A

NEK1

WDR60

SPAG1

CTU2

INTU

CCDC39

TMEM67

TRAF3IP1

GANAB

PRKCSH

RPGRIP1L

CELSR2

CPLANE1

TXNDC15

USP9X

CFTR

TBC1D32

EXOC3L2

TMEM231

CFAP298

GAS8

NPHP4

OFD1

KIF14

PIAS1

ALMS1

CEP41

HYLS1

PDE6D

PKD2

SUFU

TCTN2

CLUAP1

ALG8

FAM186B

ARL3

NEK8

NPHP1

DNAH11

DYNC2H1

C2CD3

KIAA0556

CFAP410

ZMYND10

MCIDAS

TCTEX1D2

RSPH3

IQCB1

DZIP1L

RSPH9

CEP104

TMEM216

IFT81

MAPKBP1

DNAJB13

TMEM107

TCTN3

WDR35

ANKS6

The Invitae Ciliopathies Panel analyzes genes that are associated with ciliopathy syndromes, a class of disorders that share many symptoms, including renal disease, eye defects, intellectual disability, diabetes, obesity, situs inversus, polydactyly, and a variety of skeletal dysplasias. These genes were selected based on the available evidence to date to provide a broad analysis for inherited ciliopathies.

Invitae Ciliopathies Panel

UMOD

VIPAS39

FAT4

GREB1L

SIX2

SLIT2

FOXC1

ROBO2

AGTR1

SIX5

PAX2

FRAS1

TBX18

GATA3

PBX1

CRKL

ITGA8

HOXA13

DSTYK

BICC1

EYA1

HPSE2

SIX1

BNC2

VPS33B

FREM1

SOX17

NRIP1

WNT4

LRP4

FGF20

FREM2

DCHS1

GLI3

SALL1

The Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel analyzes genes that are associated with abnormalities of the kidneys and structures of the urinary tract including bladder, ureters and urethra. CAKUT is a congenital disorder with variable severity and may go undetected until later in life. These genes were curated based on the available evidence to date to provide a broad analysis for inherited congenital anomalies of the kidney and urinary tract.

Invitae Congenital Anomalies of Kidney and Urinary Tract (CAKUT) Panel

DNAJB11

CEP89

TSC2

LRP5

SEC61A1

SEC63

INVS

DICER1

GLIS2

NPHP3

TSC1

ZNF423

NOTCH2

PKHD1

JAG1

COL4A1

TTC21B

Genetic testing for genes associated with cystic kidney disease including but not limited to Alport syndrome, focal segmental glomerulosclerosis (FSGS), and nephrotic syndrome. Cystic kidney conditions are genetically heterogeneous disorders representing a spectrum of hereditary renal conditions. The genetic heterogeneity associated with these conditions can make it difficult to use phenotype as the sole criterion to select a definitive cause. Broad panel testing allows for an efficient evaluation of several potential genes based on a single clinical indication.

Invitae Cystic Kidney Disease Panel

SLC41A1

SLX4

SMC1A

ELP1

LZTR1

GLIS3

RPL26

RPL5

The Invitae Expanded Renal Disease Panel analyzes genes that are associated with renal disorders including but not limited to Alport syndrome, focal segmental glomerulosclerosis (FSGS), nephrotic syndrome, renal tubular disorders, as well as syndromic conditions which include renal disease or renal anomalies as a clinical feature. Renal disorders are genetically heterogeneous disorders representing a wide spectrum of hereditary renal conditions. These genes were selected based on the available evidence to date to provide a broad analysis for inherited renal conditions.

Invitae Expanded Renal Disease Panel