Oncology Tests



Chromosome Analysis
  • 811 Chromosome Analysis, Unstimulated Blood, for Hematologic Disorders
  • 812 Chromosome Analysis, Bone Marrow, for Hematologic Disorders
  • 836 Chromosome Analysis, Tumor/Pleural Effusion/ Ascites fluid, for Neoplastic Disorders
Molecular Analysis
  • 887M31 RT-PCR for BCR/ABL1 Fusion Transcript, t(9;22)(q34;q11.2)
  • 887M35 RT-PCR for PML/RARA Fusion Transcript, t(15;17)(q24;q21)
  • 893M51 Quantitative PCR for BCR/ABL1, t(9;22)(q34;q11.2) Major breakpoint
  • 893M52 Quantitative PCR for BCR/ABL1, t(9;22)(q34;q11.2) minor breakpoint
  • 890ONC Illumina Microarray Analysis- Oncology
  • 840C41 Qualitative BRAF V600E [BRAF-M]
  • 840C42 Qualitative PCR for Calreticulin [CALR]
  • 840C44 Quantitative PCR for JAK2 (V617F) [JAK2MD]c43
  • 840C46 Microsatellite Instability Analysis [MSI-M]
  • 840C47 STR Engraftment- Unseparated Lineages, Bone Marrow [STREBM]
  • 840C48 STR Engraftment- Unseparated Lineages, Blood [STREWB]
  • 840C49 STR Engraftment- Separated Lineages, (CD3 (STRCD3)/, CD33 (STRCD33)) [STRSEP]
  • 840C50 RAS/RAF Targeted Gene Mutation Panel by NGS (BRAF, KRAS, HRAS, NRAS) [RASRAF]
  • 840C51 RAS/RAF/PIK Targeted Gene Mutation Panel by NGS (BRAF, KRAS, NRAS, PIK3CA) [RRPIK]
  • 840C52 Lung Cancer Mutation Panel (BRAF, KRAS, EGFR, ERBB2) [LCMP]
  • 840C53 B-Cell Clonality IGH and IGK [BCELLC]
  • 840C54 T-Cell Clonality Gamma with reflex to Beta [TCELLC]
  • 840C55 IDH1/IDH2 Mutation Analysis [IDH-M]
  • 840C40 Cancer Mutation Panel (50 Genes) [CANPNL]
    • ABL1, AKT1, ALK, APC, ATM, BRAF, CDH1, CDKN2A, CSF1R, CTNNB1,
    • EGFR, ERBB2, ERBB4, EZH2, FBXW7, FGFR1, FGFR2, FGFR3, FLT3, GNA11,
    • GNAQ, GNAS, HNF1A, HRAS, IDH1, ISH2, JAK2, JAK3, KDR, KIT,
    • KRAS, MET, MLH1, MPL, NOTCH1, NPM1, NRAS, PDGFRA, PIK3CA, PTEN,
    • PTPN11, RB1, RET, SMAD4, SMARCB1, SMO, SRC, STK11, TP53, VHL
  • 895M60 FLT3 Mutation Analysis
  • 895M61 NPM1 Mutation Analysis
  • 895M62 CEBPA Mutation Analysis
  • 895M63 KIT (C-KIT) Mutation Analysis
  • AML MUTATION ANALYSIS PANEL includes
    • 895M60 FLT3 Mutation Analysis
    • 895M61 NPM1 Mutation Analysis
    • 895M62 CEBPA Mutation Analysis
FISH Analysis Paraffin Sections (FFPE)*
  • 883 ERBB2 (HER2) Gene Amplification Status
  • 886F5 Deletion 1p36 for glial neoplasia
  • 886F6 Deletion 19q13 for glial neoplasia

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FISH Analysis (Panels)
  • MYELOMA PANEL includes
    • 882F82 IGH Gene Rearrangement, 14q32
    • 881F62 CCND1/IGH Fusion, t(11;14)(q13;q32)
    • 881F69 FGFR3/IGH Fusion, t(4;14)(p16;q32)
    • 881F70 IGH/MAF Fusion, t(14;16)(q32;q23)
    • 881F72 IGH/MAFB t(14;20)(q32;q12)
    • 870F40 11q22 Deletion/Duplication, ATM gene
    • 870F43 Deletion 13q14, D13S319
    • 870F47 Deletion 17p13.1, TP53
    • 870F55 Gain 1q21 for myeloma
  • MYELOMA HYPERDIPLOIDY PANEL includes
    • 870F45 EGR1 5q31 (for trisomy 5 detection)
    • 870F42 D7S522  7q31 (for trisomy 7 detection)
  • MDS PANEL includes
  • AML PANEL includes
    • 870F45 Deletion 5q31, EGR1
    • 870F42 Deletion 7q31, D7S522
    • 881F63 RUNX1T1/RUNX1 Fusion, t(8;21)(q22;q22)
    • 882F80 CBFB Gene Rearrangement, 16q22
    • 882F84 KMT2A (MLL) Gene Rearrangement, 11q23
  • CLL PANEL includes
    • 870F40 11q22 Deletion/Duplication, ATM gene
    • 870F43 Deletion 13q14, D13S319
    • 870F47 Deletion 17p13.1, TP53
    • 870F51 Trisomy 12, D12Z3
  • PEDIATRIC ALL PANEL includes
    • 881F67 ETV6/RUNX1 Fusion, t(12;21)(p13;q22)
    • 881F61 BCR/ABL1 Fusion, t(9;22)(q34;q11.2)
    • 870F48 Trisomy 4, CEP4
    • 870F49 Trisomy 10, CEP10
    • 870F50 Trisomy 17, D17Z1
    • 882F84 KMT2A (MLL) Gene Rearrangement, 11q23

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FISH Analysis

see also FISH probes by chromosome and FISH probes by use category including CPT codes

  • 870F40 11q22 Deletion/Duplication, ATM gene
  • 870F41 Trisomy 8, D8Z2
  • 870F42 Deletion 7q31, D7S522
  • 870F43 Deletion 13q14, D13S319
  • 870F44 Deletion 20q, D20S108
  • 870F45 Deletion 5q31, EGR1
  • 870F46 Deletion 9p21, P16
  • 870F47 Deletion 17p13.1, TP53
  • 870F48 Trisomy 4, CEP4
  • 870F49 Trisomy 10, CEP10
  • 870F50 Trisomy 17, D17Z1
  • 870F51 Trisomy 12, D12Z3
  • 870F52 X and Y sex chromosomes
  • 870F55 Gain 1q21 for myeloma
  • 881F60 AP12/MALT1 Fusion, t(11;18)(q21;q21)
  • 881F61 BCR/ABL1 Fusion, t(9;22)(q34;q11.2)
  • 881F62 CCND1/IGH Fusion, t(11;14)(q13;q32)
  • 881F63 RUNX1T1/RUNX1 Fusion, t(8;21)(q22;q22)
  • 881F64 IGH/BCL2 Fusion, t(14;18)(q32;q21) *
  • 881F65 MYC/IGH Fusion, t(8;14)(q24;q32) *
  • 881F66 PML/RARA Fusion, t(15;17)(q24;q21)
  • 881F67 ETV6/RUNX1 Fusion, t(12;21)(p13;q22)
  • 881F68 IGH/MALT1 Fusion, t(14;18)(q32;q21)
  • 881F69 FGFR3/IGH Fusion, t(4;14)(p16;q32)
  • 881F70 IGH/MAF Fusion, t(14;16)(q32;q23)
  • 881F71 BCR/ABL1+ASS Tri-color Fusion, t(9;22)
  • 881F72 IGH/MAFB t(14;20)(q32;q12)
  • 882F80 CBFB Gene Rearrangement, 16q22
  • 882F81 EWSR1 Gene Rearrangement, 22q12.2 *
  • 882F82 IGH Gene Rearrangement, 14q32 *
  • 882F83 MALT1 Gene Rearrangement, 18q21 *
  • 882F84 KMT2A (MLL) Gene Rearrangement, 11q23
  • 882F85 MYC Gene Rearrangement, 8q24 *
  • 882F86 SS18 Gene Rearrangement, 18q11.2 *
  • 882F87 ALK Gene Rearrangement, 2p23 *
  • 882F88 BCL6 Gene Rearrangement, 3q27 *
  • 882F89 FIP1L1-CHIC2-PDGFRa Gene Rearrangement 4q12
  • 882F90 PDGFRb Gene Rearrangement, 5q33
  • 882F91 TRA/D Gene Rearrangement, 14q11.2
  • 882F92 RARA Gene Rearrangement, 17q21
  • 882F93 FGFR1 Gene Rearrangement, 8p11
  • 882F94 DDIT3 (CHOP) Gene Rearrangement, 12q13 *
  • 882F95 FUS Gene Rearrangement, 16p11 *

 red asterisk * denotes probes also validated for use on FFPE

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