LOC101928682 uncharacterized LOC101928682

Information
Symbol
LOC101928682
Type
ncRNA
Description
uncharacterized LOC101928682
Entrez Gene ID
101928682
Genome
hg19
Position
chr16:87,300,864-87,326,044
Genome
hg38
Position
chr16:87,267,258-87,292,438
Ensembl
ENSG00000261697 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 ENSG00000261697 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000570286.5 hg38 chr16 87,262,759 87,292,438 29,680
ENST00000569872.1 hg38 chr16 87,267,258 87,292,438 25,181
ENST00000561709.1 hg38 chr16 87,271,907 87,292,409 20,503
ENST00000570286.5 hg19 chr16 87,296,365 87,326,044 29,680
ENST00000569872.1 hg19 chr16 87,300,864 87,326,044 25,181
ENST00000561709.1 hg19 chr16 87,305,513 87,326,015 20,503
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