LOC105376020 uncharacterized LOC105376020

Information
Symbol
LOC105376020
Type
ncRNA
Description
uncharacterized LOC105376020
Entrez Gene ID
105376020
Genome
hg19
Position
chr9:33,401,519-33,410,548
Genome
hg38
Position
chr9:33,401,521-33,410,550
Ensembl
ENSG00000286322 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
Ensembl ENSG00000286322 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000664487.1 hg38 chr9 33,401,677 33,410,553 8,877
ENST00000688867.1 hg38 chr9 33,401,521 33,410,550 9,030
ENST00000450864.1 hg38 chr9 33,402,857 33,409,948 7,092
ENST00000688867.1 hg19 chr9 33,401,519 33,410,548 9,030
ENST00000664487.1 hg19 chr9 33,401,675 33,410,551 8,877
ENST00000450864.1 hg19 chr9 33,402,855 33,409,946 7,092
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