LOC105373383 uncharacterized LOC105373383

Information
Symbol
LOC105373383
Type
ncRNA
Description
uncharacterized LOC105373383
Entrez Gene ID
105373383
Genome
hg19
Position
chrX:152,864,770-152,874,716
Genome
hg38
Position
chrX:153,599,315-153,609,261
Ensembl
ENSG00000293160 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 ENSG00000293160 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000642834.1 hg38 chrX 153,599,315 153,609,261 9,947
ENST00000646177.1 hg38 chrX 153,599,443 153,613,937 14,495
ENST00000642692.1 hg38 chrX 153,599,363 153,607,986 8,624
ENST00000642834.1 hg19 chrX 152,864,770 152,874,716 9,947
ENST00000642692.1 hg19 chrX 152,864,818 152,873,441 8,624
ENST00000646177.1 hg19 chrX 152,864,898 152,879,392 14,495
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