Hs04021774_cn

• Gene Symbol: CEACAM19
• Assay Reference Genome Location: Chr.19:44675362 on build GRCh38
• Cytoband: 19q13.31

Target Gene Details

• Entrez Gene ID: 56971
• Gene Name: carcinoembryonic antigen related cell adhesion molecule 19
• Gene Aliases: CEACM19, CEAL1
• Location: Chr.19:44671452-44684355 on Build GRCh38
• Assay Gene Location: Within Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
CEACAM19	NM_001127893.1			NP_001121365.1
	NM_020219.3			NP_064604.2
	AK027157.1
	AK291588.1
	AY358394.1			AAQ88760.1
	BC083499.1			AAH83499.1
	KJ851726.1
	KJ851727.1
	KJ851728.1
	KJ851729.1
	KJ851730.1
	KJ851731.1
	KJ851732.1
	KJ851733.1
	KJ851734.1
	KJ851735.1
	KJ851736.1
	KJ851737.1
	KJ851738.1
	KJ851739.1
	KJ851740.1
	KJ851741.1
	KJ851742.1
	KJ851743.1
	KJ851744.1
	KJ851745.1
	KJ851746.1
	KJ851747.1
	KJ851748.1
	KJ851749.1
	KJ851750.1
	KJ851751.1
	KJ851752.1
	KJ851753.1
	KJ851754.1
	KJ851755.1
	KJ851756.1
	KJ851757.1
	KJ851758.1
	KJ851759.1
	KJ851760.1
	KJ851761.1
	KJ851762.1
	KJ851763.1
	KJ851764.1
	KJ851765.1
	KJ851766.1
	KJ851767.1
	KJ851768.1
	KJ851769.1
	KJ851770.1
	KJ851771.1
	KJ851772.1
	KJ851773.1
	KJ851774.1
	KJ851775.1
	KJ851776.1
	KJ851777.1
	KJ851778.1
	KJ851779.1
	KJ851780.1
	KJ851781.1
	KJ851782.1
	KJ851783.1
KJ851784.1
KJ851785.1
KJ851786.1
KJ851787.1
KJ851788.1
KJ851789.1
KJ851790.1
KJ851791.1
KJ851792.1
KJ851793.1
KJ851794.1
KJ851795.1
KJ851796.1
KJ851797.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv9737	Chr.19:44674838 - 44703359 on Build GRCh38	Gain	CEACAM19 CEACAM16
nsv1062812	Chr.19:44538275 - 44711525 on Build GRCh38	Gain	CEACAM22P PVR CEACAM19 IGSF23 MIR4531 CEACAM16
nsv483005	Chr.19:44530751 - 44705087 on Build GRCh38	Loss	CEACAM22P PVR CEACAM19 IGSF23 MIR4531 CEACAM16

More Information

Additional Information:

For this assay, SNP(s) [rs112723153] 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