LOC101927769 uncharacterized LOC101927769

Information
Symbol
LOC101927769
Type
ncRNA
Description
uncharacterized LOC101927769
Entrez Gene ID
101927769
Genome
hg19
Position
chr7:20,336,261-20,351,340
Genome
hg38
Position
chr7:20,296,638-20,311,717
Ensembl
ENSG00000226097 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 ENSG00000226097 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000446399.6 hg38 chr7 20,296,638 20,311,717 15,080
ENST00000664310.1 hg38 chr7 20,296,637 20,314,512 17,876
ENST00000669469.1 hg38 chr7 20,296,687 20,314,483 17,797
ENST00000453564.1 hg38 chr7 20,298,294 20,300,625 2,332
ENST00000664310.1 hg19 chr7 20,336,260 20,354,135 17,876
ENST00000446399.6 hg19 chr7 20,336,261 20,351,340 15,080
ENST00000669469.1 hg19 chr7 20,336,310 20,354,106 17,797
ENST00000453564.1 hg19 chr7 20,337,917 20,340,248 2,332
Genome browser