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11q22 deletion/duplication, FISH, ATM gene
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1q21 gain, FISH, CKS1B gene
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ABL1 Rearrangement, FISH
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ABL2 Rearrangement, FISH
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ALL FISH Panel
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ALL High Risk Pediatric FISH Panel
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AML FISH Panel
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API2/MALT1 Fusion, t(11;18)(q21;q21), FISH
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BCL2 Rearrangement, FISH
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BCL6 Rearrangement, FISH
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BCR/ABL1 Fusion Transcript, t(9;22)(q34;q11.2), RT-PCR
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BCR/ABL1 Fusion, t(9;22)(q34;q11.2), FISH
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BCR/ABL1 PCR -M, t(9;22)(q34;q11.2), Monitoring
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BCR/ABL1 PCR-D, t(9;22)(q34;q11.2), Diagnostic sample
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BCR/ABL1,ASS Tri-color Fusion, FISH, t(9;22)(q34;q11.2)
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BRAF Rearrangement, FISH
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CBFB Rearrangement, inv(16)(p13.1q22), FISH
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CCND1/IgH Fusion, t(11;14)(q13;q32), FISH
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CLL FISH Panel
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CRLF2 Rearrangement, FISH
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Chromosome Analysis, Amniotic Fluid, for Prenatal Genetic Diagnosis
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Chromosome Analysis, Amniotic Fluid-Abridged, for Pre-natal Genetic Diagnosis
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Chromosome Analysis, Blood, Abridged Examination for Familial Chromosome Rearrangements
|
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Chromosome Analysis, Blood, for Genetic Diagnosis
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Chromosome Analysis, Bone Marrow, for Hematologic Disorders
|
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Chromosome Analysis, Chorionic Villus Sample, for Prenatal Genetic Diagnosis
|
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Chromosome Analysis, Chorionic Villus Sample-Abridged, for Pre-natal Genetic Diagnosis
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Chromosome Analysis, Products of Conception/Tissue Biopsy, for Genetic Diagnosis
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Chromosome Analysis, Tumor/Pleural Effusion/Ascites fluid, for Neoplastic Disorders
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Chromosome Analysis, Unstimulated Blood, for Hematologic Disorders
|
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Core Binding Factor FISH Panel
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DDIT3 (CHOP) Rearrangement, FISH, 12q13
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DNA Isolation and Banking
|
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DNA Isolation and one year storage
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Deletion 13q14, FISH, D13S319
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Deletion 17p13.1, FISH, TP53
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Deletion 19q, FISH, Glial neoplasia
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Deletion 1p, FISH, Glial neoplasia
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Deletion 20q, FISH, D20S108
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Deletion 5q31, Monosomy 5, FISH, EGR1
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Deletion 7q31, Monosomy 7, FISH, D7S522
|
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Deletion 9p21, FISH, P16
|
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DiGeorge/Velo-cardio-facial/Shprintzen/Conotruncal anomaly syndrome, Deletion 22q11.2, TUPLE1, FISH, for Genetic Diagnosis
|
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ERBB2 (HER2) Gene Amplification status, FISH
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ETV6/RUNX1 (TEL/AML1) Fusion, t(12;21)(p13;q22), FISH
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EWSR1 Rearrangement, FISH
|
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FGFR1 Rearrangement, FISH, 8p11
|
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FGFR3/IgH Fusion, t(4;14)(p16;q32), FISH
|
|
FIP1L1-CHIC2-PDGFRA Rearrangement, FISH
|
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FUS Rearrangement, FISH, 16p11
|
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Familial Mutation, Targeted Sequencing (TVARFAM)
|
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Fragile X Analysis, Molecular Diagnosis
|
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IGH Rearrangement, FISH
|
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IGH/BCL2 Fusion, t(14;18)(q32;q21), FISH
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IGH/MAF Fusion, t(14;16)(q32;q23), FISH
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IGH/MAFB Fusion, t(14;20)(q32;q12), FISH
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IGH/MALT1 Fusion, t(14;18)(q32;q21), FISH
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|
Illumina Microarray Analysis
|
|
Illumina Microarray Analysis - Oncology
|
|
Illumina Microarray Analysis- Targeted Family
|
|
KMT2A [MLL] Rearrangement, FISH
|
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MALT1 Rearrangement, FISH
|
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MDM2 Gene Amplification status, FISH
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MDS FISH Panel
|
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MECOM Rearrangement, FISH
|
|
MYC Rearrangement, FISH
|
|
MYC/IgH Fusion, t(8;14)(q24;q32), FISH
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Methylation Specific PCR, SNRPN gene, 15q
|
|
Myeloma FISH panel
|
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Myeloma Hyperdiploidy FISH Panel
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NUP98 Rearrangement, FISH
|
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PDGFRB Rearrangement, FISH
|
|
PML/RARA Fusion Transcript, t(15;17)(q24;q21), RT-PCR
|
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PML/RARA Fusion, t(15;17)(q24;q21), FISH
|
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PlainSEEK Panel
|
|
Prenatal Aneuploidy Panel, FISH, Amniotic fluid
|
|
RARA Rearrangement, FISH, 17q21
|
|
RUNX1T1/RUNX1 (ETO/AML1) Fusion, t(8;21)(q22;q22), FISH
|
|
SRY (Sex determining Region on Y), Yp11.3, FISH, for Genetic Diagnosis
|
|
SS18 (SYT) Rearrangement, FISH
|
|
Stillbirth Aneuploidy Panel, FISH, Paraffin embedded fetal tissue
|
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Sudden Unexplained Death in the Young (SUDY) Exome
|
|
TCR Rearrangement (TRA/D), FISH
|
|
Targeted Variant Analysis via Sanger DNA Sequencing
|
|
Tissue Culture and Shipment
|
|
Trisomy 10, FISH, CEP10
|
|
Trisomy 12, FISH, D12Z3
|
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Trisomy 17, FISH, D17Z1
|
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Trisomy 4, FISH, CEP4
|
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Trisomy 8, FISH, D8Z2
|
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Whole Exome Sequencing: Duo Analysis
|
|
Whole Exome Sequencing: Proband Analysis Only
|
|
Whole Exome Sequencing: Trio Analysis
|
|
X and Y sex chromosomes, FISH, DXZ1 and DYZ3
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