CBX7 chromobox 7

Information
Symbol
CBX7
Type
protein-coding
Description
chromobox 7
Entrez Gene ID
23492
Genome
hg19
Position
chr22:39,526,777-39,548,685
Genome
hg38
Position
chr22:39,130,772-39,152,680
MIM
608457 OMIM
HGNC
HGNC:1557 HGNC
Ensembl
ENSG00000100307 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 2
Uncertain significance 0 22
Ranking
ClinVar
0
0
0
22
2
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 608457 OMIM
HGNC HGNC:1557 HGNC
Ensembl ENSG00000100307 Ensembl
AllianceGenome HGNC:1557
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000401405.7 hg38 chr22 39,133,584 39,152,444 18,861
ENST00000216133.10 hg38 chr22 39,130,772 39,152,680 21,909
ENST00000216133.10 hg19 chr22 39,526,777 39,548,685 21,909
ENST00000401405.7 hg19 chr22 39,529,589 39,548,449 18,861
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