Hs04955595_cn

• Gene Symbol: ST7
• Assay Reference Genome Location: Chr.7:116974070 on build GRCh38
• Cytoband: 7q31.2

Target Gene Details

• Entrez Gene ID: 7982
• Gene Name: suppression of tumorigenicity 7
• Gene Aliases: ETS7q, FAM4A, FAM4A1, HELG, RAY1, SEN4, TSG7
• Location: Chr.7:116953327-117230023 on Build GRCh38
• Assay Gene Location: Within Intron 1

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
ST7	NM_018412.3			NP_060882.2
	NM_021908.2			NP_068708.1
	AF234882.1			AAF85945.1
	AF234883.1			AAF85946.1
	AK292372.1
	AK298540.1
	BC030954.1			AAH30954.1
	BC075855.1			AAH75855.1
	KJ534947.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
dgv1324e214	Chr.7:116905405 - 117056329 on Build GRCh38	Gain	MIR6132 ST7-OT4 CAPZA2 ST7-AS1 ST7
esv3891196	Chr.7:116905706 - 117032710 on Build GRCh38	Gain	MIR6132 ST7-OT4 CAPZA2 ST7-AS1 ST7
nsv981571	Chr.7:116968895 - 116977025 on Build GRCh38	Duplication	ST7
esv3614704	Chr.7:116947077 - 117046223 on Build GRCh38	Gain	MIR6132 ST7-OT4 ST7-AS1 ST7
nsv831107	Chr.7:116774680 - 117009412 on Build GRCh38	Gain	ST7-OT4 CAPZA2 ST7-AS1 ST7 MET

More Information

Additional Information:

For this assay, SNP(s) [rs114703959] 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