For your convenience, we’ve provided below a list of the CPT and ICD-10 codes for the clinical and laboratory services offered at Insight Medical Genetics.

 

Cancer (most common tests are listed below, more available)

GENE/DISORDERCODE(S)
BRCA 1/2 Sequencing and Del/Dup81162
BRCA 1/2 Ashkenazi Target81212
Lynch Syndrome81292
81295
81298
81294
81297
81300
81403
81317
81319

 

Consultation

SERVICECODE(S)
MD and Genetic Counselor99243 or 99244 or 99245
Genetic Counseling OnlyS0265

 

First Trimester Screening

SERVICECODE(S)
Cell-free DNA (NIPT)81425
81507
Cell-free DNA (NIPT)(Blood Draw and Ultrasound) with Counseling81425
81507
36415
76801
76813
S0265 or 99243
First Trimester Screening (Blood and Ultrasound) with Counseling81512
36415
76801
76813
S0265 or 99243
First Trimester Screening (blood draw only)81512
Ultrasound(s)76801
76813
(add 76802 and 76814 for twins)

 

NextGen Panel Testing

DISORDERCODE(S)
Noonan Panel81442
Noonan Panel - Targeted81406
Osteogenesis Imperfecta/Skeletal Dysplasia Panel81404(x2)
81405(x2)
81406(x2)
81408(x2)
Osteogenesis Imperfecta - Targeted81406

 

Single Gene/Carrier Screening

GENE/DISORDERCODE(S)
ACADM81406
Beta Thalassemia and other beta- globinopathies 81364
81363
Canavan Disease 81406
CFTR Del/Dup 81223
81400
81401
Cystic Fibrosis Sequencing 81223
81224
Congenital Disorder of Glycosylation Type 1A 81406
CPT II Deficiency 81404
Familial Mediterranean Fever 81404
Fragile X 81244
Fundamental Panel (CF, SMA, Fragile X Only) 81223
81400
81401
81257
81259
81363
81364
Gaucher Disease Sequencing (GBA Gene Sequencing) 81261
GJB2 and GJB681252
81254
Glycogen Storage Disease Type 1A81404
Hereditary Fructosuria - ALDO B 81406
Hex A Tay-Sachs 81406
IMG Extended Carrier Screening (Includes SMA-GT, FX, GJB6, GBA) 81223
81364
81243
81401
81404
81405
81406
81407
81408
Miscellaneous genetic testing 81479
Pompe disease 81406
SCAD: Short Chain acyl-CoA dehydrogenase deficiency 81405
SMA - Deletion and Genotyping (IMG)81400
81401
SMA Genotyping 81401
Smith Lemli Opitz - DHCR781405
Spinal Muscular Atrophy (SMN 1) 81405
Targeted Sequencing 81403
Tay-Sachs Enzyme Testing 81406

 

Other Testing

SERVICECODE(S)
Amniocentesis specimen testing (Does not include Microarray)88267
88235(x2)
88280
88291
82106
88377(x2)
Blood Draw36415
CVS specimen testing (Does not include Microarray88267
88235(x2)
88280
88291
82106
88377(x2)
81265
Fluorescence In-Situ Hybridization (FISH) Only88291
88273
88368
88369
Karyotyping88230(x2)
88262
88291
Maternal Cell Contamination Studies (MCC)81265
81266 (for multiples)
Microarray and MCC 81229
81265
81266 (for multiples)
Microarray - fetal sample81229
81265
POC-188230(x2)
88267
88280
88285
88291
88381