Hs00417865_cn

• Gene Symbol: DMWD
• Assay Reference Genome Location: Chr.19:45785925 on build GRCh38
• Cytoband: 19q13.32

Target Gene Details

• Entrez Gene ID: 1762
• Gene Name: dystrophia myotonica, WD repeat containing
• Gene Aliases: D19S593E, DMR-N9, DMRN9, gene59
• Location: Chr.19:45783006-45792802 on Build GRCh38
• Assay Gene Location: Within Exon 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
DMWD	NM_004943.1	3	1617	NP_004934.1
	BC019266.1	1	700	AAH19266.1
	BT006798.1	1	626	AAP35444.1
	CD106470.1	1	270
	L19267.1	3	1205	AAA35767.1

Target Copy Number Variation Details

• DGV Version: Release date: 2016-05-15, GRCh GRCh38

Target Variation	Location	CNV Subtype	Genes
nsv579870	Chr.19:45704552 - 45814335 on Build GRCh38	Loss	SIX5 RSPH6A FBXO46 DMWD DMPK BHMG1

More Information

• Set Membership: Intragenic, Exonic, DGV Variation

Gene Ontology Categories:

Function(s)

molecular_function