Cytogenetics & flow cytometry in Jammu
Karyotype, FISH and flow-cytometry tests used to diagnose and monitor blood cancers and related disorders. 37 tests available through Jammu Genetics Hub in Jammu — open any test to see what it is for, who it is advised for, its sample type and partner-lab price.
14q32 (IGH) translocation (FFPE Tissue Block)
14q32 (IGH) translocation (FFPE Tissue Block) is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
17p (TP53) Deletion By FISH
17p (TP53) Deletion By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations…
6q Deletion By FISH
6q Deletion By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
CD19 By Flowcytometry
CD19 By Flowcytometry is a flow cytometry (immunophenotyping) test used in cancer diagnosis. Flow cytometry identifies cell types from the proteins on their surface — classifying leukemias and…
CD20 By Flowcytometry
CD20 By Flowcytometry is a flow cytometry (immunophenotyping) test used in cancer diagnosis. Flow cytometry identifies cell types from the proteins on their surface — classifying leukemias and…
CEP 8, Trisomy 8 By FISH
CEP 8, Trisomy 8 By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions…
Chromosomal Breakage Studies in Fanconi’s Anemia/Aplastic Anemia
Chromosomal Breakage Studies in Fanconi’s Anemia/Aplastic Anemia is a conventional karyotyping (chromosome analysis) test used in cancer diagnosis.
cMYC Breakapart By FISH
cMYC Breakapart By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions…
del (17p) Analysis
del (17p) Analysis is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
del(17p13) :TP53 deletion analysis
del(17p13) :TP53 deletion analysis is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
Deletion 20Q By FISH
Deletion 20Q By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
Deletion 5Q By FISH
Deletion 5Q By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
Deletion 7Q By FISH
Deletion 7Q By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
Deletion/Monosomy 5 By FISH
Deletion/Monosomy 5 By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations…
Deletion/Monosomy 7 By FISH
Deletion/Monosomy 7 By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations…
DiGeorge Syndrome By FISH
DiGeorge Syndrome By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions…
FISH for IGH translocation/rearrangement
FISH for IGH translocation/rearrangement is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
FISH for IGH Translocation/Rearrangement (FFPE)
FISH for IGH Translocation/Rearrangement (FFPE) is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
Flowcytometry For CD34
Flowcytometry For CD34 is a flow cytometry (immunophenotyping) test used in cancer diagnosis. Flow cytometry identifies cell types from the proteins on their surface — classifying leukemias and…
IGH Gene Rearrangement By FISH
IGH Gene Rearrangement By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations…
Iso 17q By FISH
Iso 17q By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or extra…
Karyotyping: Hematologic Malignancy
Karyotyping: Hematologic Malignancy is a conventional karyotyping (chromosome analysis) test used in cancer diagnosis.
MET1 Amplification
MET1 Amplification is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
PDGFR Alpha (4q12) Gene Rearrangement By FISH
PDGFR Alpha (4q12) Gene Rearrangement By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
PDGFR Beta (5q33) Gene Rearrangement By FISH
PDGFR Beta (5q33) Gene Rearrangement By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
PML Ra Ra t(15;17) By FISH
PML Ra Ra t(15;17) By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations…
PML Ra Ra t(15;17), Qualitative
PML Ra Ra t(15;17), Qualitative is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations…
PML Ra Ra t(15;17), Quantitative
PML Ra Ra t(15;17), Quantitative is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
T-Cell Receptor Gene Rearrangement, PCR, Blood
T-Cell Receptor Gene Rearrangement, PCR, Blood is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
TCRA/D (14q11.2) Gene Rearrangement By FISH
TCRA/D (14q11.2) Gene Rearrangement By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
TP53 deletion: del(17)(p13.1) [FFPE]
TP53 deletion: del(17)(p13.1) [FFPE] is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis.
Trisomy 11 By FISH
Trisomy 11 By FISH is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
Trisomy 21 Analysis
Trisomy 21 Analysis is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
Trisomy 3
Trisomy 3 is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or extra gene…
Trisomy 5,9 & 15
Trisomy 5,9 & 15 is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or extra…
Trisomy 7
Trisomy 7 is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or extra gene…
Trisomy 8 Analysis
Trisomy 8 Analysis is a FISH (fluorescence in-situ hybridisation) test used in cancer diagnosis. FISH uses fluorescent probes to find specific chromosome changes — translocations, deletions or…
Questions about this test? Talk to us.
Our team can explain what a test measures, what sample is needed and how your report reaches you. For inherited cancer risk, Jammu Genetics Hub also helps patients in Jammu connect with BGCI-certified geneticists before and after testing. Test choices for a cancer diagnosis are best made with your oncologist.