NES nestin

Information
Symbol
NES
Type
protein-coding
Description
nestin
Entrez Gene ID
10763
Genome
hg19
Position
chr1:156,638,555-156,647,199
Genome
hg38
Position
chr1:156,668,763-156,677,407
MIM
600915 OMIM
HGNC
HGNC:7756 HGNC
Ensembl
ENSG00000132688 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 18
Likely benign 0 38
Uncertain significance 0 172
Ranking
ClinVar
0
0
6
222
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
SYNONYM Nbla00170
MIM 600915 OMIM
HGNC HGNC:7756 HGNC
Ensembl ENSG00000132688 Ensembl
AllianceGenome HGNC:7756
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000368223.4 hg38 chr1 156,668,763 156,677,407 8,645
ENST00000368223.4 hg19 chr1 156,638,555 156,647,199 8,645
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