LINC02682 long intergenic non-protein coding RNA 2682

Information
Symbol
LINC02682
Type
ncRNA
Description
long intergenic non-protein coding RNA 2682
Entrez Gene ID
105376570
Genome
hg19
Position
chr11:15,932,495-15,945,960
Genome
hg38
Position
chr11:15,910,949-15,924,414
HGNC
HGNC:54177 HGNC
Ensembl
ENSG00000254661 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
SYNONYM lnc-SOX6-1
HGNC HGNC:54177 HGNC
Ensembl ENSG00000254661 Ensembl
AllianceGenome HGNC:54177
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000670379.1 hg38 chr11 15,910,944 15,924,012 13,069
ENST00000670509.1 hg38 chr11 15,910,949 15,924,414 13,466
ENST00000668712.1 hg38 chr11 15,910,930 15,927,511 16,582
ENST00000664116.1 hg38 chr11 15,910,948 15,930,951 20,004
ENST00000668712.1 hg19 chr11 15,932,476 15,949,057 16,582
ENST00000670379.1 hg19 chr11 15,932,490 15,945,558 13,069
ENST00000664116.1 hg19 chr11 15,932,494 15,952,497 20,004
ENST00000670509.1 hg19 chr11 15,932,495 15,945,960 13,466
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