Hs06452441_cn

• Gene Symbol: FAM69C
• Assay Reference Genome Location: Chr.18:74456742 on build GRCh38
• Cytoband: 18q22.3

Target Gene Details

• Entrez Gene ID: 125704
• Gene Name: family with sequence similarity 69 member C
• Gene Aliases: C18orf51
• Location: Chr.18:74432575-74464646 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM69C	NM_001044369.2			NP_001037834.2
	XM_017025551.1			XP_016881040.1
	BC019628.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv577653	Chr.18:74436411 - 74471994 on Build GRCh38	Gain	FAM69C
nsv1057441	Chr.18:74344906 - 74669985 on Build GRCh38	Gain	LINC00909 CNDP1 LOC101927606 C18orf63 FAM69C ZNF407 CNDP2
esv3643117	Chr.18:74454714 - 74614537 on Build GRCh38	Loss	LINC00909 CNDP1 FAM69C ZNF407 CNDP2
nsv577654	Chr.18:74445966 - 74467617 on Build GRCh38	Gain	FAM69C
nsv527671	Chr.18:74415709 - 74476151 on Build GRCh38	Gain	FAM69C
esv1000434	Chr.18:74422735 - 74465401 on Build GRCh38	Deletion	FAM69C

More Information

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