VSTM2B-DT VSTM2B divergent transcript

Information
Symbol
VSTM2B-DT
Type
ncRNA
Description
VSTM2B divergent transcript
Entrez Gene ID
284395
Genome
hg19
Position
chr19:29,777,918-30,016,659
Genome
hg38
Position
chr19:29,287,011-29,525,752
HGNC
HGNC:27615 HGNC
Ensembl
ENSG00000264515 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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
HGNC HGNC:27615 HGNC
Ensembl ENSG00000264515 Ensembl
AllianceGenome HGNC:27615
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000660387.1 hg38 chr19 29,287,032 29,398,856 111,825
ENST00000582581.5 hg38 chr19 29,287,011 29,525,752 238,742
ENST00000582581.5 hg19 chr19 29,777,918 30,016,659 238,742
ENST00000660387.1 hg19 chr19 29,777,939 29,889,763 111,825
Genome browser