Hs03568613_cn

• Gene Symbol: FAM193B
• Assay Reference Genome Location: Chr.5:177532189 on build GRCh38
• Cytoband: 5q35.3

Target Gene Details

• Entrez Gene ID: 54540
• Gene Name: family with sequence similarity 193 member B
• Gene Aliases: IRIZIO
• Location: Chr.5:177519789-177554585 on Build GRCh38
• Assay Gene Location: Overlaps Intron 7 - Exon 8

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM193B	NM_001190946.2			NP_001177875.1
	NR_024019.3
	XM_006714875.2			XP_006714938.1
	XM_006714876.1			XP_006714939.1
	XM_006714878.1			XP_006714941.1
	XM_006714879.3			XP_006714942.1
	XM_006714880.1			XP_006714943.1
	XM_006714884.1			XP_006714947.1
	XM_006714885.1			XP_006714948.1
	XM_006714886.2			XP_006714949.1
	XM_011534572.1			XP_011532874.1
	XM_011534573.1			XP_011532875.1
	XM_011534574.1			XP_011532876.1
	XM_011534579.2			XP_011532881.1
	XM_011534580.1			XP_011532882.1
	XM_011534581.1			XP_011532883.1
	XM_011534582.1			XP_011532884.1
	XM_011534583.1			XP_011532885.1
	AB067518.1			BAB67824.1
	AK001266.1			BAA91589.1
	AK096032.1
	BC008784.2			AAH08784.1
	BC071696.1			AAH71696.1
	BX431446.2
	BX647587.1			CAI46078.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv5148	Chr.5:177519430 - 177552310 on Build GRCh38	Insertion	FAM193B
nsv5147	Chr.5:177511195 - 177556017 on Build GRCh38	Deletion	DDX41 FAM193B
nsv1161311	Chr.5:177305104 - 177546474 on Build GRCh38	Duplication	DDX41 DOK3 LMAN2 F12 MXD3 PRR7 PRR7-AS1 PFN3 PRELID1 PDLIM7 SLC34A1 GRK6 FAM193B RGS14 DBN1

More Information

Additional Information:

For this assay, SNP(s) [rs77949511] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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