LOC100506271 uncharacterized LOC100506271

Information
Symbol
LOC100506271
Type
ncRNA
Description
uncharacterized LOC100506271
Entrez Gene ID
100506271
Genome
hg19
Position
chr22:37,748,230-37,751,337
Genome
hg38
Position
chr22:37,352,190-37,355,297
Ensembl
ENSG00000237862 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 ENSG00000237862 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000666674.1 hg38 chr22 37,352,190 37,355,002 2,813
ENST00000445088.2 hg38 chr22 37,352,190 37,355,297 3,108
ENST00000700412.1 hg38 chr22 37,339,569 37,353,618 14,050
ENST00000700412.1 hg19 chr22 37,735,610 37,749,658 14,049
ENST00000666674.1 hg19 chr22 37,748,230 37,751,042 2,813
ENST00000445088.2 hg19 chr22 37,748,230 37,751,337 3,108
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