LOC101928782 uncharacterized LOC101928782

Information
Symbol
LOC101928782
Type
ncRNA
Description
uncharacterized LOC101928782
Entrez Gene ID
101928782
Genome
hg19
Position
chr7:131,594,979-131,633,712
Genome
hg38
Position
chr7:131,910,220-131,948,953
Ensembl
ENSG00000224865 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 ENSG00000224865 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000415393.1 hg38 chr7 131,910,220 131,948,953 38,734
ENST00000656736.1 hg38 chr7 131,897,289 131,898,212 924
ENST00000656736.1 hg19 chr7 131,582,048 131,582,971 924
ENST00000415393.1 hg19 chr7 131,594,979 131,633,712 38,734
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