Hs06861565_cn

• Gene Symbol: B4GALT1-AS1
• Assay Reference Genome Location: Chr.9:33174252 on build GRCh38
• Cytoband: 9p21.1

Target Gene Details

• Entrez Gene ID: 101929639
• Gene Name: B4GALT1 antisense RNA 1
• Gene Aliases: -
• Location: Chr.9:33166948-33179983 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
B4GALT1-AS1	NR_108108.1
	NR_108109.1
	NR_108110.1
	AB371488.1
	HY028011.1
	HY043002.1
	HY143413.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv519369	Chr.9:33134619 - 33283163 on Build GRCh38	Gain	CHMP5 B4GALT1 B4GALT1-AS1 SPINK4 BAG1
dgv7515n100	Chr.9:33042019 - 33241605 on Build GRCh38	Gain	SMU1 B4GALT1 B4GALT1-AS1 SPINK4
dgv7516n100	Chr.9:33121909 - 33278846 on Build GRCh38	Gain	CHMP5 B4GALT1 B4GALT1-AS1 SPINK4 BAG1
esv2762813	Chr.9:33139254 - 33261075 on Build GRCh38	Gain	B4GALT1 B4GALT1-AS1 SPINK4 BAG1

More Information

Additional Information:

For this assay, SNP(s) [rs373804504] 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