LOC100506937 uncharacterized LOC100506937

Information
Symbol
LOC100506937
Type
ncRNA
Description
uncharacterized LOC100506937
Entrez Gene ID
100506937
Genome
hg19
Position
chr7:132,443,730-132,445,392
Genome
hg38
Position
chr7:132,758,970-132,760,632
Ensembl
ENSG00000225881 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 ENSG00000225881 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000663581.1 hg38 chr7 132,758,992 132,760,616 1,625
ENST00000436379.1 hg38 chr7 132,758,970 132,760,632 1,663
ENST00000436379.1 hg19 chr7 132,443,730 132,445,392 1,663
ENST00000663581.1 hg19 chr7 132,443,752 132,445,376 1,625
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