DSCR9 Down syndrome critical region 9

Information
Symbol
DSCR9
Type
ncRNA
Description
Down syndrome critical region 9
Entrez Gene ID
257203
Genome
hg19
Position
chr21:38,580,804-38,594,037
Genome
hg38
Position
chr21:37,208,503-37,221,736
HGNC
HGNC:16301 HGNC
Ensembl
ENSG00000230366 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 NCRNA00038
HGNC HGNC:16301 HGNC
Ensembl ENSG00000230366 Ensembl
AllianceGenome HGNC:16301
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000715704.1 hg38 chr21 37,208,234 37,216,541 8,308
ENST00000715705.1 hg38 chr21 37,208,275 37,216,674 8,400
ENST00000454482.2 hg38 chr21 37,208,503 37,221,736 13,234
ENST00000585273.5 hg38 chr21 37,208,503 37,220,696 12,194
ENST00000581640.5 hg38 chr21 37,208,503 37,220,688 12,186
ENST00000715704.1 hg19 chr21 38,580,535 38,588,842 8,308
ENST00000715705.1 hg19 chr21 38,580,576 38,588,975 8,400
ENST00000581640.5 hg19 chr21 38,580,804 38,592,989 12,186
ENST00000585273.5 hg19 chr21 38,580,804 38,592,997 12,194
ENST00000454482.2 hg19 chr21 38,580,804 38,594,037 13,234
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