Hs05347680_cn

• Gene Symbol: FAM227B
• Assay Reference Genome Location: Chr.15:49380634 on build GRCh38
• Cytoband: 15q21.2

Target Gene Details

• Entrez Gene ID: 196951
• Gene Name: family with sequence similarity 227 member B
• Gene Aliases: C15orf33
• Location: Chr.15:49326997-49620931 on Build GRCh38
• Assay Gene Location: Within Intron 17

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM227B	NM_152647.2			NP_689860.2
	XM_005254213.3			XP_005254270.1
	XM_005254214.3			XP_005254271.1
	XM_005254215.3			XP_005254272.1
	XM_005254216.3			XP_005254273.1
	XM_005254219.3			XP_005254276.1
	XM_006720423.2			XP_006720486.1
	XM_006720424.2			XP_006720487.1
	XM_006720426.2			XP_006720489.1
	XM_006720427.3			XP_006720490.1
	XM_011521319.2			XP_011519621.1
	XM_011521320.1			XP_011519622.1
	XM_011521321.2			XP_011519623.1
	XM_011521322.1			XP_011519624.1
	XM_017021990.1			XP_016877479.1
	XM_017021991.1			XP_016877480.1
	XM_017021992.1			XP_016877481.1
	XM_017021993.1			XP_016877482.1
	XM_017021994.1			XP_016877483.1
	XM_017021995.1			XP_016877484.1
	XM_017021996.1			XP_016877485.1
	AK057362.1			BAB71451.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3636427	Chr.15:49359900 - 49397828 on Build GRCh38	Loss	FAM227B GALK2
nsv833002	Chr.15:49329203 - 49489602 on Build GRCh38	Gain	FGF7 FAM227B GALK2
nsv442375	Chr.15:49360327 - 49391885 on Build GRCh38	Loss	FAM227B GALK2
esv3636426	Chr.15:49354085 - 49408851 on Build GRCh38	Loss	FAM227B GALK2

More Information

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