Product Details

Assay Reference Genome
Location

Chr.8:31060692 on build GRCh38
Cytoband
8p12
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

Target Gene Details

Entrez Gene ID
7486
Gene Symbol
WRN
Gene Name
Werner syndrome RecQ like helicase
Gene Aliases
RECQ3, RECQL2, RECQL3
Location
Chr.8:31033262-31173761 on build GRCh38
Assay Gene Location
Within Intron 3
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
WRN NM_000553.4 NP_000544.2
XM_011544639.2 XP_011542941.1
AF091214.1 AAC63361.1
AY818673.1
BP279291.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv831278 Chr8:31059468 - 31213390 on Build GRCh38 Gain WRN

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