LOC105370169 uncharacterized LOC105370169

Information
Symbol
LOC105370169
Type
ncRNA
Description
uncharacterized LOC105370169
Entrez Gene ID
105370169
Genome
hg19
Position
chr13:39,627,176-39,671,331
Genome
hg38
Position
chr13:39,053,039-39,097,194
Ensembl
ENSG00000273507 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 ENSG00000273507 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000654394.1 hg38 chr13 39,053,072 39,091,661 38,590
ENST00000655342.1 hg38 chr13 39,053,073 39,223,238 170,166
ENST00000661973.2 hg38 chr13 39,053,039 39,097,194 44,156
ENST00000661973.2 hg19 chr13 39,627,176 39,671,331 44,156
ENST00000654394.1 hg19 chr13 39,627,209 39,665,798 38,590
ENST00000655342.1 hg19 chr13 39,627,210 39,797,375 170,166
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