LOC101928438 uncharacterized LOC101928438

Information
Symbol
LOC101928438
Type
ncRNA
Description
uncharacterized LOC101928438
Entrez Gene ID
101928438
Genome
hg19
Position
chr9:102,159,269-102,582,203
Genome
hg38
Position
chr9:99,396,987-99,819,921
Ensembl
ENSG00000237461 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 ENSG00000237461 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000427039.1 hg38 chr9 99,585,786 99,819,889 234,104
ENST00000652827.1 hg38 chr9 99,396,987 99,819,921 422,935
ENST00000701763.1 hg38 chr9 99,717,544 99,819,895 102,352
ENST00000652827.1 hg19 chr9 102,159,269 102,582,203 422,935
ENST00000427039.1 hg19 chr9 102,348,068 102,582,171 234,104
ENST00000701763.1 hg19 chr9 102,479,826 102,582,177 102,352
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