LOC100996437 uncharacterized LOC100996437

Information
Symbol
LOC100996437
Type
ncRNA
Description
uncharacterized LOC100996437
Entrez Gene ID
100996437
Genome
hg19
Position
chr7:66,134,341-66,136,510
Genome
hg38
Position
chr7:66,669,354-66,671,523
Ensembl
ENSG00000226824 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 ENSG00000226824 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000657342.1 hg38 chr7 66,654,578 66,670,413 15,836
ENST00000448096.1 hg38 chr7 66,654,538 66,666,299 11,762
ENST00000662347.1 hg38 chr7 66,669,354 66,671,523 2,170
ENST00000448096.1 hg19 chr7 66,119,525 66,131,286 11,762
ENST00000657342.1 hg19 chr7 66,119,565 66,135,400 15,836
ENST00000662347.1 hg19 chr7 66,134,341 66,136,510 2,170
Genome browser