CD37 CD37 molecule

Information
Symbol
CD37
Type
protein-coding
Description
CD37 molecule
Entrez Gene ID
951
Genome
hg19
Position
chr19:49,838,663-49,843,863
Genome
hg38
Position
chr19:49,335,406-49,340,606
MIM
151523 OMIM
HGNC
HGNC:1666 HGNC
Ensembl
ENSG00000104894 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 6
Likely benign 0 2
Uncertain significance 0 12
Ranking
ClinVar
0
0
0
20
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 :
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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
SYNONYM GP52-40
SYNONYM TSPAN26
MIM 151523 OMIM
HGNC HGNC:1666 HGNC
Ensembl ENSG00000104894 Ensembl
AllianceGenome HGNC:1666
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000535669.6 hg38 chr19 49,335,427 49,340,205 4,779
ENST00000323906.9 hg38 chr19 49,335,406 49,340,606 5,201
ENST00000598095.5 hg38 chr19 49,335,396 49,340,132 4,737
ENST00000426897.6 hg38 chr19 49,335,396 49,340,575 5,180
ENST00000598095.5 hg19 chr19 49,838,653 49,843,389 4,737
ENST00000426897.6 hg19 chr19 49,838,653 49,843,832 5,180
ENST00000323906.9 hg19 chr19 49,838,663 49,843,863 5,201
ENST00000535669.6 hg19 chr19 49,838,684 49,843,462 4,779
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