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See other C21ORF58 CNV Assays ›
Gene Symbol
C21orf58
Assay Reference Genome
Location

Chr.21:46315036 on build GRCh38
Cytoband
21q22.3
Assay ID Hs01110133_cn
Size
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Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 54058

Gene Name:

 chromosome 21 open reading frame 58

Gene Aliases:

 -

Location:

 Chr.21:46300426-46323899 on Build GRCh38

Assay Gene Location:

 Overlaps Intron 7 - Exon 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
C21orf58 NM_001286462.1 NP_001273391.1
NM_001286463.1 NP_001273392.1
NM_001286476.1 NP_001273405.1
NM_001286477.1 NP_001273406.1
NM_058180.4 NP_478060.2
XM_005261148.4 XP_005261205.1
XM_006724018.3 XP_006724081.1
XM_011529619.2 XP_011527921.1
XM_011529620.2 XP_011527922.1
XM_011529621.2 XP_011527923.1
XM_011529623.2 XP_011527925.1
XM_011529624.2 XP_011527926.1
XM_011529625.2 XP_011527927.1
XM_011529626.2 XP_011527928.1
XM_011529627.2 XP_011527929.1
XM_017028388.1 XP_016883877.1
XM_017028389.1 XP_016883878.1
XM_017028390.1 XP_016883879.1
XM_017028391.1 XP_016883880.1
XM_017028392.1 XP_016883881.1
XM_017028393.1 XP_016883882.1
AK056387.1
AK096641.1
AK098098.1 BAC05232.1
AY039243.1 AAK72408.1
AY039244.1 AAK72409.1
BC121007.1
BC121008.1 4 2014

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv3547 Chr.21:46283787 - 46321516 on Build GRCh38 Insertion C21orf58 MCM3AP YBEY
nsv519904 Chr.21:46163592 - 46461396 on Build GRCh38 Loss PCNT C21orf58 LSS MCM3AP SPATC1L MCM3AP-AS1 YBEY DIP2A
nsv527355 Chr.21:46258860 - 46443112 on Build GRCh38 Gain PCNT C21orf58 MCM3AP YBEY
nsv470910 Chr.21:45933861 - 46665076 on Build GRCh38 Gain PCNT LOC101928796 C21orf58 LSS COL6A1 S100B PCBP3 COL6A2 DIP2A-IT1 PRMT2 FTCD MCM3AP SPATC1L MCM3AP-AS1 YBEY DIP2A
nsv587975 Chr.21:46241321 - 46410929 on Build GRCh38 Gain PCNT C21orf58 MCM3AP MCM3AP-AS1 YBEY
nsv1060978 Chr.21:46068159 - 46413726 on Build GRCh38 Gain PCNT C21orf58 LSS FTCD MCM3AP SPATC1L MCM3AP-AS1 YBEY COL6A2

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

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