KBTBD6-DT KBTBD6 divergent transcript

Information
Symbol
KBTBD6-DT
Type
ncRNA
Description
KBTBD6 divergent transcript
Entrez Gene ID
101929140
Genome
hg19
Position
chr13:41,707,075-41,810,822
Genome
hg38
Position
chr13:41,132,939-41,236,686
HGNC
HGNC:56824 HGNC
Ensembl
ENSG00000278390 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:56824 HGNC
Ensembl ENSG00000278390 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000619407.4 hg38 chr13 41,132,939 41,236,686 103,748
ENST00000661006.1 hg38 chr13 41,132,952 41,236,655 103,704
ENST00000615685.4 hg38 chr13 41,132,959 41,192,835 59,877
ENST00000620300.5 hg38 chr13 41,132,952 41,176,310 43,359
ENST00000660769.2 hg38 chr13 41,132,928 41,146,646 13,719
ENST00000660769.2 hg19 chr13 41,707,064 41,720,782 13,719
ENST00000619407.4 hg19 chr13 41,707,075 41,810,822 103,748
ENST00000620300.5 hg19 chr13 41,707,088 41,750,446 43,359
ENST00000661006.1 hg19 chr13 41,707,088 41,810,791 103,704
ENST00000615685.4 hg19 chr13 41,707,095 41,766,971 59,877
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