LINC01791 long intergenic non-protein coding RNA 1791

Information
Symbol
LINC01791
Type
ncRNA
Description
long intergenic non-protein coding RNA 1791
Entrez Gene ID
107985312
Genome
hg19
Position
chr19:31,658,363-31,660,521
Genome
hg38
Position
chr19:31,167,457-31,169,615
HGNC
HGNC:52581 HGNC
Ensembl
ENSG00000267777 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
HGNC HGNC:52581 HGNC
Ensembl ENSG00000267777 Ensembl
AllianceGenome HGNC:52581
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000660210.1 hg38 chr19 31,167,457 31,169,615 2,159
ENST00000589511.1 hg38 chr19 31,167,516 31,207,663 40,148
ENST00000659731.1 hg38 chr19 31,167,513 31,225,143 57,631
ENST00000655296.1 hg38 chr19 31,167,486 31,207,654 40,169
ENST00000671470.1 hg38 chr19 31,167,502 31,207,646 40,145
ENST00000660210.1 hg19 chr19 31,658,363 31,660,521 2,159
ENST00000655296.1 hg19 chr19 31,658,392 31,698,560 40,169
ENST00000671470.1 hg19 chr19 31,658,408 31,698,552 40,145
ENST00000659731.1 hg19 chr19 31,658,419 31,716,049 57,631
ENST00000589511.1 hg19 chr19 31,658,422 31,698,569 40,148
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