LOC101928392 uncharacterized LOC101928392

Information
Symbol
LOC101928392
Type
ncRNA
Description
uncharacterized LOC101928392
Entrez Gene ID
101928392
Genome
hg19
Position
chr16:82,525,343-82,609,095
Genome
hg38
Position
chr16:82,491,738-82,575,490
Ensembl
ENSG00000261285 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 ENSG00000261285 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000565374.2 hg38 chr16 82,553,894 82,575,518 21,625
ENST00000568136.5 hg38 chr16 82,495,993 82,510,896 14,904
ENST00000650164.1 hg38 chr16 82,491,738 82,575,490 83,753
ENST00000650164.1 hg19 chr16 82,525,343 82,609,095 83,753
ENST00000568136.5 hg19 chr16 82,529,598 82,544,501 14,904
ENST00000565374.2 hg19 chr16 82,587,499 82,609,123 21,625
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