Hs02211862_cn

• Gene Symbol: FAM69C
• Assay Reference Genome Location: Chr.18:74435824 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 Exon 6

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM69C	NM_001044369.2	4	1946	NP_001037834.2
	XM_011525816.2	4	1992	XP_011524118.1
	XM_017025551.1	4	1872	XP_016881040.1
	AI375747.1	1	103
	BC019628.1	3	1233

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv3401n100	Chr.18:74355436 - 74453287 on Build GRCh38	Gain	C18orf63 FAM69C LOC101927606
nsv1057441	Chr.18:74344906 - 74669985 on Build GRCh38	Gain	C18orf63 CNDP1 ZNF407 FAM69C LINC00909 CNDP2 LOC101927606
nsv527671	Chr.18:74415709 - 74476151 on Build GRCh38	Gain	FAM69C
esv3643115	Chr.18:74369739 - 74453340 on Build GRCh38	Loss	FAM69C LOC101927606
nsv1067091	Chr.18:74424482 - 74442193 on Build GRCh38	Loss	FAM69C
esv1000434	Chr.18:74422735 - 74465401 on Build GRCh38	Deletion	FAM69C

More Information

• Set Membership: Intragenic, Exonic, DGV Variation