LOC101928335 uncharacterized LOC101928335

Information
Symbol
LOC101928335
Type
ncRNA
Description
uncharacterized LOC101928335
Entrez Gene ID
101928335
Genome
hg19
Position
chrX:107,137,820-107,179,406
Genome
hg38
Position
chrX:107,894,590-107,936,176
Ensembl
ENSG00000236064 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 ENSG00000236064 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000700938.1 hg38 chrX 107,858,526 107,936,210 77,685
ENST00000670461.1 hg38 chrX 107,894,738 107,935,980 41,243
ENST00000430140.3 hg38 chrX 107,894,590 107,936,176 41,587
ENST00000700938.1 hg19 chrX 107,101,756 107,179,440 77,685
ENST00000430140.3 hg19 chrX 107,137,820 107,179,406 41,587
ENST00000670461.1 hg19 chrX 107,137,968 107,179,210 41,243
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