Hs05105119_cn

• Gene Symbol: CCDC7
• Assay Reference Genome Location: Chr.10:32565968 on build GRCh38
• Cytoband: 10p11.22

Target Gene Details

• Entrez Gene ID: 79741
• Gene Name: coiled-coil domain containing 7
• Gene Aliases: BIOT2, BioT2-A, BioT2-B, BioT2-C, C10orf68
• Location: Chr.10:32446082-32882864 on Build GRCh38
• Assay Gene Location: Within Intron 20

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CCDC7	NM_001026383.2			NP_001021554.1
	NM_001321115.1			NP_001308044.1
	NM_145023.5			NP_659460.3
	NR_109826.1
	XM_006717505.1			XP_006717568.1
	XM_006717506.1			XP_006717569.1
	XM_011519663.1			XP_011517965.1
	XM_011519664.1			XP_011517966.1
	XM_011519666.1			XP_011517968.1
	XM_011519667.1			XP_011517969.1
	XM_011519668.1			XP_011517970.1
	XM_011519669.1			XP_011517971.1
	XM_011519670.1			XP_011517972.1
	XM_011519671.1			XP_011517973.1
	XM_011519672.1			XP_011517974.1
	XM_011519673.1			XP_011517975.1
	XM_011519674.1			XP_011517976.1
	XM_011519675.1			XP_011517977.1
	XM_011519676.1			XP_011517978.1
	XM_011519677.1			XP_011517979.1
	XM_011519678.1			XP_011517980.1
	XM_011519679.1			XP_011517981.1
	XM_011519680.2			XP_011517982.1
	XM_011519683.2			XP_011517985.1
	XM_011519684.2			XP_011517986.1
	XM_011519685.1			XP_011517987.1
	XM_011519686.2			XP_011517988.1
	XM_011519688.2			XP_011517990.1
	XM_017016638.1			XP_016872127.1
	XM_017016639.1			XP_016872128.1
	XM_017016640.1			XP_016872129.1
	XM_017016641.1			XP_016872130.1
	XM_017016642.1			XP_016872131.1
	XM_017016643.1			XP_016872132.1
	XM_017016644.1			XP_016872133.1
	XM_017016645.1			XP_016872134.1
	XM_017016646.1			XP_016872135.1
	XM_017016647.1			XP_016872136.1
	XM_017016648.1			XP_016872137.1
	XM_017016649.1			XP_016872138.1
	XM_017016650.1			XP_016872139.1
	XM_017016651.1			XP_016872140.1
	XM_017016652.1			XP_016872141.1
	AK057324.1			BAB71426.1
	AK058148.1			BAB71686.1
	BC022020.2			AAH22020.2
	BC042672.1			AAH42672.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
esv3891783	Chr.10:32542994 - 32621788 on Build GRCh38	Gain	CCDC7

More Information

Additional Information:

For this assay, SNP(s) [rs73253465] 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