Hs07224232_cn

• Gene Symbol: FAM209B
• Assay Reference Genome Location: Chr.20:56534219 on build GRCh38
• Cytoband: 20q13.31

Target Gene Details

• Entrez Gene ID: 388799
• Gene Name: family with sequence similarity 209 member B
• Gene Aliases: C20orf107, dJ1153D9.4
• Location: Chr.20:56527124-56555626 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM209B	NM_001013646.3			NP_001013668.2
	XM_017027849.1			XP_016883338.1
	BC105792.1			AAI05793.1
	DB452055.1
	DB517586.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2722576	Chr.20:56526267 - 56536764 on Build GRCh38	Deletion	FAM209A FAM209B
nsv525425	Chr.20:56403979 - 56897294 on Build GRCh38	Gain	FAM209A FAM209B LOC105372682 CASS4 GCNT7 RTFDC1 TFAP2C CSTF1
nsv834015	Chr.20:56518712 - 56656502 on Build GRCh38	Loss	FAM209A FAM209B LOC105372682 GCNT7 RTFDC1 TFAP2C
nsv1056574	Chr.20:56495687 - 56761211 on Build GRCh38	Gain	FAM209A FAM209B LOC105372682 GCNT7 RTFDC1 TFAP2C

More Information

• Set Membership: Intragenic, Intronic, Non-exonic, DGV Variation