Hs03585416_cn

• Gene Symbol: FAM8A1
• Assay Reference Genome Location: Chr.6:17605690 on build GRCh38
• Cytoband: 6p22.3

Target Gene Details

• Entrez Gene ID: 51439
• Gene Name: family with sequence similarity 8 member A1
• Gene Aliases: AHCP
• Location: Chr.6:17600287-17611719 on Build GRCh38
• Assay Gene Location: Within Intron 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM8A1	NM_016255.2			NP_057339.1
	AF097027.1			AAF07850.1
	AK296393.1
	AK307681.1
	AK312814.1
	BC047881.1			AAH47881.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv5922n100	Chr.6:17490857 - 17921391 on Build GRCh38	Gain	CAP2 LOC101928491 NUP153 KIF13A LOC105374952 FAM8A1
esv2731633	Chr.6:17602713 - 17605882 on Build GRCh38	Deletion	FAM8A1
nsv516012	Chr.6:17459945 - 17876993 on Build GRCh38	Gain+Loss	CAP2 LOC101928491 NUP153 KIF13A LOC105374952 FAM8A1
nsv601046	Chr.6:17492862 - 17893291 on Build GRCh38	Gain	CAP2 LOC101928491 NUP153 KIF13A LOC105374952 FAM8A1
dgv1715e212	Chr.6:17457368 - 17679729 on Build GRCh38	Gain	CAP2 LOC101928491 NUP153 FAM8A1
nsv830596	Chr.6:17597791 - 17767811 on Build GRCh38	Gain	NUP153 KIF13A LOC105374952 FAM8A1
nsv1027813	Chr.6:17457369 - 17630059 on Build GRCh38	Gain	CAP2 LOC101928491 NUP153 FAM8A1

More Information

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