FISH Probes by usage type and by Test Code

Test Description Test Code CPT Codes

Oncology
ATM (11q22) Deletion/duplication of ATM 870F40 88271, 88275
8 Centromere Trisomy 8 870F41 88271, 88275
7q31 (D7S522) Deletion 7q / Monosomy 7 870F42 88271, 88271, 88275
13q14 (D13S319) Deletion 13q / Monosomy 13 870F43 88271, 88271, 88275
20q12 (D20S108) Deletion 20q 870F44 88271, 88275
5q31 (EGR1) Deletion 5q / Monosomy 5 870F45 88271, 88271, 88275
9p21 (P16) Deletion 9p 870F46 88271, 88275
17p13.1 (TP53) Deletion 17p 870F47 88271, 88275
4 Centromere Trisomy 4 870F48 88271, 88275
10 Centromere Trisomy 10 870F49 88271, 88275
17 Centromere Trisomy 17 870F50 88271, 88275
12 Centromere Trisomy 12 870F51 88271, 88275
X, Y Centromeres Sex chromosomes 870F52 88271, 88271, 88275
1q gain Gain of 1q detection for myeloma 870F55 88271, 88271, 88275
API1/MALT1 fusion t(11;18)(q21;q21) 881F60 88271, 88271, 88275
BCR/ABL1 fusion t(9;22)(q34;q11.2) 881F61 88271, 88271, 88275
CCND1/IGH fusion t(11;14)(q13;q32) 881F62 88271, 88271, 88275
RUNX1T1/RUNX1 (ETO/AML1) fusion t(8;21)(q22;q22) 881F63 88271, 88271, 88275
IGH/BCL2 fusion t(14;18)(q32;q21) 881F64 88271, 88271, 88275
MYC/IGH fusion t(8;14)(q24;q32) 881F65 88271, 88271, 88275
PML/RARA fusion t(15;17)(q24;q21) 881F66 88271, 88271, 88275
ETV6/RUNX1 (TEL/AML1) fusion t(12;21)(p13;q22) 881F67 88271, 88271, 88275
IGH/MALT1 fusion t(14;18)(q32;q21) 881F68 88271, 88271, 88275
FGFR3/IGH fusion t(4;14)(p16;q32) 881F69 88271, 88271, 88275
IGH/MAF fusion t(14;16)(q32;q23) 881F70 88271, 88271, 88275
BCR/ABL1/ASS fusion t(9;22)(q34;q11.2)/ASS deletion 881F71 88271, 88271, 88271, 88275
IGH/MAFB fusion t(14;20)(q32;q12) 881F72 88271, 88271, 88275
NUP98 gene rearrangement 11p15.4 882F78 88271, 88271, 88275
MECOM gene rearrangement 3q26.2 882F79 88271, 88271, 88275
CBFB gene rearrangement 16q22 [inversion 16] 882F80 88271, 88271, 88275
EWSR1 gene rearrangement 22q12.2 [Ewing’s sarcoma] 882F81 88271, 88271, 88275
IGH gene rearrangement 14q32 882F82 88271, 88271, 88275
MALT1 gene rearrangement 18q21 [MALT lymphoma] 882F83 88271, 88271, 88275
KMT2A (MLL) gene rearrangement 11q23 882F84 88271, 88271, 88275
MYC gene rearrangement 8q24 882F85 88271, 88271, 88275
SS18 gene rearrangement 18q11.2 [Synovial sarcoma] 882F86 88271, 88271, 88275
BCL6 gene rearrangement 3q27 882F88 88271, 88271, 88275
FIP1L1/CHIC2/PDGFRa gene rearr. 4q12 882F89 88271, 88271, 88271, 88275
PDGFRb gene rearrangement 5q33 882F90 88271, 88271, 88275
TRA/D (T-cell receptor alpha/delta) gene rearr. 14q11.2 882F91 88271, 88271, 88275
RARA gene rearrangement 17q21 882F92 88271, 88271, 88275
FGFR1 gene rearrangement 8p11 882F93 88271, 88271, 88275
DDIT3 (CHOP) gene rearrangement 12q13 882F94 88271, 88271, 88275
FUS gene rearrangement 16p11 882F95 88271, 88271, 88275
BCL2 gene rearrangement 18q21.22 882F96  88271, 88271, 88275
CRLF2 gene rearrangement Xp22.33/Yp11.23 882F97 88271, 88271, 88275
ABL1 gene rearrangement 9q34 882F98 88271, 88271, 88275
ABL2 gene rearrangement 1q25.2 882F98 88271, 88271, 88275
ERBB2 (HER2) ERBB2 gene amplification status 883 83950

1p36/19q13 deletion

 (ordered together)

 Deletion detection for glial neoplasia 886F5, 886F6

88271, 88271, 88275

88271, 88271, 88275

Constitutional
DiGeorge/VCF/Schpritzen Conotruncal Anomaly Syndrome, TUPLE1 Deletion 22q11.2 871F28 88271, 88273
SRY, (Sex Determining Region of Y) Deletion Yp11.3 871F34 88271, 88273

Prenatal
Prenatal Aneuploidy Panel, Amniotic fluid 13q, 18cen, 21q, Xcen, Ycen 873 88271×5, 88275
Stillbirth Aneuploidy Panel, Paraffin embedded 13q, 16cen, 18cen, 21q, 22q, Xcen, Ycen 875 88271×7, 88275

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