PDGFRB PDGFRB FUSIONS Detail (hg19) (PDGFRB)

Information

Genome

Assembly Position
hg19 chr5:149,493,402-149,535,408
 
hg38 chr5:150,113,839-150,155,845 View the variant detail on this assembly version.
 
Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics Show details

ClinVar

Clinical Significance
Review star [No Data.]
Show details
Links
Type Database ID Link
Gene MIM 173410 OMIM
HGNC 8804 HGNC
Ensembl ENSG00000113721 Ensembl
NCBI NCBI
Gene Cards Gene Cards
OncoKB OncoKB
Type Database ID Link
Variant TogoVar
COSMIC
MONDO
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
Disease Drug EL ET ED CS VO TR Pubmed Links
chronic myelomonocytic leukemia A Diagnostic Supports Negative Somatic 5 27069254 Detail
hematologic cancer A Diagnostic Supports Positive Somatic 5 27069254 Detail
myeloproliferative neoplasm Imatinib A Predictive Supports Sensitivity/Response Somatic 4 16960151 Detail
DisGeNET
[No Data.]
Annotation

Annotations

DescrptionSourceLinks
The 2016 World Health Organization guidelines for the classification of myeloid malignancies uses th... CIViC Evidence Detail
The 2016 World Health Organization guidelines for the classification of myeloid malignancies and acu... CIViC Evidence Detail
Twelve patients with BCR-ABL-negative chronic myeloproliferative disease and reciprocal translocatio... CIViC Evidence Detail
Gene
PDGFRB
Genome
hg19
Position
chr5:149,493,402-149,535,408
Variant Type
fusion
Variant (CIViC) (CIViC Variant)
PDGFRB FUSIONS
Variant URL (CIViC Variant)
https://civic.genome.wustl.edu/links/variants/568
Genome browser