LOC100505851 uncharacterized LOC100505851

Information
Symbol
LOC100505851
Type
ncRNA
Description
uncharacterized LOC100505851
Entrez Gene ID
100505851
Genome
hg19
Position
chr19:24,101,883-24,140,732
Genome
hg38
Position
chr19:23,919,081-23,957,930
Ensembl
ENSG00000269289 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 ENSG00000269289 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598914.2 hg38 chr19 23,949,575 23,958,035 8,461
ENST00000596326.5 hg38 chr19 23,919,081 23,957,930 38,850
ENST00000596326.5 hg19 chr19 24,101,883 24,140,732 38,850
ENST00000598914.2 hg19 chr19 24,132,377 24,140,837 8,461
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