LOC102723968 uncharacterized LOC102723968

Information
Symbol
LOC102723968
Type
ncRNA
Description
uncharacterized LOC102723968
Entrez Gene ID
102723968
Genome
hg19
Position
chr13:64,402,980-64,417,574
Genome
hg38
Position
chr13:63,828,847-63,843,441
Ensembl
ENSG00000290964 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 ENSG00000290964 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000641745.1 hg38 chr13 63,837,295 63,843,424 6,130
ENST00000607822.5 hg38 chr13 63,828,847 63,843,441 14,595
ENST00000606050.1 hg38 chr13 63,828,847 63,844,125 15,279
ENST00000607822.5 hg19 chr13 64,402,980 64,417,574 14,595
ENST00000606050.1 hg19 chr13 64,402,980 64,418,258 15,279
ENST00000641745.1 hg19 chr13 64,411,428 64,417,557 6,130
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