Hs05343851_cn

• Gene Symbol: IQCH
• Assay Reference Genome Location: Chr.15:67283635 on build GRCh38
• Cytoband: 15q23

Target Gene Details

• Entrez Gene ID: 64799
• Gene Name: IQ motif containing H
• Gene Aliases: NYDSP5
• Location: Chr.15:67254772-67501804 on Build GRCh38
• Assay Gene Location: Within Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
IQCH	NM_001031715.2			NP_001026885.1
	NM_001284347.1			NP_001271276.1
	NM_001284348.1			NP_001271277.1
	NM_001284349.1			NP_001271278.1
	NM_001322470.1			NP_001309399.1
	NM_001322471.1			NP_001309400.1
	NM_001322472.1			NP_001309401.1
	NM_001322473.1			NP_001309402.1
	NM_001322474.1			NP_001309403.1
	NM_001322475.1			NP_001309404.1
	NM_022784.2			NP_073621.2
	XM_011521907.2			XP_011520209.1
	XM_011521908.2			XP_011520210.1
	XM_011521911.2			XP_011520213.1
	XM_011521912.2			XP_011520214.1
	XM_011521913.2			XP_011520215.1
	XM_011521914.2			XP_011520216.1
	XM_011521915.2			XP_011520217.1
	XM_011521916.2			XP_011520218.1
	XM_011521917.2			XP_011520219.1
	XM_011521918.2			XP_011520220.1
	XM_011521922.2			XP_011520224.1
	XM_011521923.2			XP_011520225.1
	XM_017022491.1			XP_016877980.1
	XM_017022492.1			XP_016877981.1
	XM_017022493.1			XP_016877982.1
	XM_017022494.1			XP_016877983.1
	XM_017022495.1			XP_016877984.1
	XM_017022496.1			XP_016877985.1
	XM_017022497.1			XP_016877986.1
	XM_017022498.1			XP_016877987.1
	XM_017022499.1			XP_016877988.1
	XM_017022500.1			XP_016877989.1
	XM_017022501.1			XP_016877990.1
	XM_017022502.1			XP_016877991.1
	XM_017022503.1			XP_016877992.1
	XM_017022504.1			XP_016877993.1
	AK022538.1			BAB14087.1
	AK292478.1
	AK304303.1
	AY014282.2			AAK27307.2
	BC031041.1			AAH31041.2
	BC039292.1			AAH39292.1
	BC048964.1			AAH48964.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv1049980	Chr.15:67241206 - 67285222 on Build GRCh38	Loss	AAGAB IQCH

More Information

Additional Information:

For this assay, SNP(s) [rs74020133] 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, Intronic, Non-exonic, DGV Variation