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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