CBX6 chromobox 6

Information
Symbol
CBX6
Type
protein-coding
Description
chromobox 6
Entrez Gene ID
23466
Genome
hg19
Position
chr22:39,257,427-39,268,221
Genome
hg38
Position
chr22:38,861,422-38,872,216
MIM
617438 OMIM
HGNC
HGNC:1556 HGNC
Ensembl
ENSG00000183741 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 2
Uncertain significance 0 36
Ranking
ClinVar
0
0
2
36
0
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
MIM 617438 OMIM
HGNC HGNC:1556 HGNC
Ensembl ENSG00000183741 Ensembl
AllianceGenome HGNC:1556
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000216083.6 hg38 chr22 38,864,229 38,872,216 7,988
ENST00000407418.8 hg38 chr22 38,861,422 38,872,216 10,795
ENST00000407418.8 hg19 chr22 39,257,427 39,268,221 10,795
ENST00000216083.6 hg19 chr22 39,260,234 39,268,221 7,988
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