CPT directory
Pathology and Laboratory80000–89999
Pathology and laboratory procedures in the CPT code set.
1,671 active directory codes · Updated from published source data daily
Codes (100)
- 81298Msh6 gene full seq
- 81299Msh6 gene known variants
- 81300Msh6 gene dup/delete variant
- 81301Microsatellite instability
- 81302Mecp2 gene full seq
- 81303Mecp2 gene known variant
- 81304Mecp2 gene dup/delet variant
- 81305Myd88 gene p.leu265pro vrnt
- 81306Nudt15 gene common variants
- 81307Palb2 gene full gene seq
- 81308Palb2 gene known famil vrnt
- 81309Pik3ca gene trgt seq alys
- 81310Npm1 gene
- 81311Nras gene variants exon 2&3
- 81312Pabpn1 gene detc abnor allel
- 81313Pca3/klk3 antigen
- 81314Pdgfra gene
- 81315Pml/raralpha com breakpoints
- 81316Pml/raralpha 1 breakpoint
- 81317Pms2 gene full seq analysis
- 81318Pms2 known familial variants
- 81319Pms2 gene dup/delet variants
- 81320Plcg2 gene common variants
- 81321Pten gene full sequence
- 81322Pten gene known fam variant
- 81323Pten gene dup/delet variant
- 81324Pmp22 gene dup/delet
- 81325Pmp22 gene full sequence
- 81326Pmp22 gene known fam variant
- 81327Sept9 gen prmtr mthyltn alys
- 81328Slco1b1 gene com variants
- 81329Smn1 gene dos/deletion alys
- 81330Smpd1 gene common variants
- 81331Snrpn/ube3a gene
- 81332Serpina1 gene
- 81333Tgfbi gene common variants
- 81334Runx1 gene targeted seq alys
- 81335Tpmt gene com variants
- 81336Smn1 gene full gene sequence
- 81337Smn1 gen nown famil seq vrnt
- 81338Mpl gene common variants
- 81339Mpl gene seq alys exon 10
- 81340Trb@ gene rearrange amplify
- 81341Trb@ gene rearrange dirprobe
- 81342Trg gene rearrangement anal
- 81343Ppp2r2b gen detc abnor allel
- 81344Tbp gene detc abnor alleles
- 81345Tert gene targeted seq alys
- 81346Tyms gene com variants
- 81347Sf3b1 gene common variants
- 81348Srsf2 gene common variants
- 81349Cytog alys chrml abnr lw-ps
- 81350Ugt1a1 gene common variants
- 81351Tp53 gene full gene sequence
- 81352Tp53 gene trgt sequence alys
- 81353Tp53 gene known famil vrnt
- 81354Cytog alys chrml abnor ogm
- 81355Vkorc1 gene
- 81357U2af1 gene common variants
- 81360Zrsr2 gene common variants
- 81361Hbb gene com variants
- 81362Hbb gene known fam variant
- 81363Hbb gene dup/del variants
- 81364Hbb full gene sequence
- 81370Hla i & ii typing lr
- 81371Hla i & ii type verify lr
- 81372Hla i typing complete lr
- 81373Hla i typing 1 locus lr
- 81374Hla i typing 1 antigen lr
- 81375Hla ii typing ag equiv lr
- 81376Hla ii typing 1 locus lr
- 81377Hla ii type 1 ag equiv lr
- 81378Hla i & ii typing hr
- 81379Hla i typing complete hr
- 81380Hla i typing 1 locus hr
- 81381Hla i typing 1 allele hr
- 81382Hla ii typing 1 loc hr
- 81383Hla ii typing 1 allele hr
- 81400Mopath procedure level 1
- 81401Mopath procedure level 2
- 81402Mopath procedure level 3
- 81403Mopath procedure level 4
- 81404Mopath procedure level 5
- 81405Mopath procedure level 6
- 81406Mopath procedure level 7
- 81407Mopath procedure level 8
- 81408Mopath procedure level 9
- 81410Aortic dysfunction/dilation
- 81411Aortic dysfunction/dilation
- 81412Ashkenazi jewish assoc dis
- 81413Car ion chnnlpath inc 10 gns
- 81414Car ion chnnlpath inc 2 gns
- 81415Exome sequence analysis
- 81416Exome sequence analysis
- 81417Exome re-evaluation
- 81418Rx metab gen seq alys pnl 6
- 81419Epilepsy gen seq alys panel
- 81420Fetal chrmoml aneuploidy
- 81422Fetal chrmoml microdeltj
- 81425Genome sequence analysis
