Hs04955643_cn

• Gene Symbol: FAM71F2
• Assay Reference Genome Location: Chr.7:128673254 on build GRCh38
• Cytoband: 7q32.1

Target Gene Details

• Entrez Gene ID: 346653
• Gene Name: family with sequence similarity 71 member F2
• Gene Aliases: FAM137B
• Location: Chr.7:128671628-128702262 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM71F2	NM_001012454.5			NP_001012457.3
	NM_001128926.3			NP_001122398.1
	NM_001290254.1			NP_001277183.1
	NM_001290255.1			NP_001277184.1
	XM_011516128.2			XP_011514430.1
	XM_011516129.2			XP_011514431.1
	XM_011516130.2			XP_011514432.1
	XM_011516131.2			XP_011514433.1
	XM_011516132.2			XP_011514434.1
	XM_011516134.2			XP_011514436.1
	XM_011516135.2			XP_011514437.1
	XM_011516136.2			XP_011514438.1
	XM_017012147.1			XP_016867636.1
	XM_017012149.1			XP_016867638.1
	BC047310.1			AAH47310.2
	BC066973.1			AAH66973.2
	BC105729.1
	BC105730.1
	BC105731.1
	BI828876.1
	HY039605.1
	HY046252.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv2670312	Chr.7:128499519 - 128999613 on Build GRCh38	Deletion	METTL2B FLNC CCDC136 FAM71F2 LOC100130705 IRF5 LINC01000 TNPO3 OPN1SW ATP6V1F FAM71F1 KCP CALU
esv2735137	Chr.7:128499440 - 128999664 on Build GRCh38	Deletion	METTL2B FLNC CCDC136 FAM71F2 LOC100130705 IRF5 LINC01000 TNPO3 OPN1SW ATP6V1F FAM71F1 KCP CALU

More Information

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