Hs02624527_cn

• Gene Symbol: FAM188B
• Assay Reference Genome Location: Chr.7:30778572 on build GRCh38
• Cytoband: 7p14.3

Target Gene Details

• Entrez Gene ID: 84182
• Gene Name: family with sequence similarity 188 member B
• Gene Aliases: C7orf67
• Location: Chr.7:30771417-30892387 on Build GRCh38
• Assay Gene Location: Overlaps Exon 2 - Intron 2

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM188B	NM_032222.2			NP_115598.2
	AF538962.1			AAQ10898.1
	AK026027.1			BAB15327.1
	BC098569.1			AAH98569.1
	DA868176.1

Target Gene Details

• Entrez Gene ID: 100526825
• Gene Name: INMT-FAM188B readthrough (NMD candidate)
• Gene Aliases: -
• Location: Chr.7:30752135-30892387 on Build GRCh38
• Assay Gene Location: Overlaps Exon 4 - Intron 4

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
INMT-FAM188B	NR_037598.1
	AK308762.1

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv606507	Chr.7:30755672 - 30801825 on Build GRCh38	Loss	FAM188B INMT-FAM188B INMT
nsv1025945	Chr.7:30774889 - 30796411 on Build GRCh38	Loss	FAM188B INMT-FAM188B
dgv6316n100	Chr.7:30609596 - 31145482 on Build GRCh38	Gain	CRHR2 AQP1 FAM188B INMT-FAM188B GARS INMT GHRHR ADCYAP1R1
nsv830938	Chr.7:30644614 - 30857907 on Build GRCh38	Gain	CRHR2 FAM188B INMT-FAM188B INMT
nsv527038	Chr.7:30617851 - 31122331 on Build GRCh38	Gain	CRHR2 AQP1 FAM188B INMT-FAM188B GARS INMT GHRHR ADCYAP1R1
esv2761316	Chr.7:30615466 - 31127062 on Build GRCh38	Gain	CRHR2 AQP1 FAM188B INMT-FAM188B GARS INMT GHRHR ADCYAP1R1
nsv606508	Chr.7:30772130 - 30797387 on Build GRCh38	Loss	FAM188B INMT-FAM188B
nsv830939	Chr.7:30704855 - 30871891 on Build GRCh38	Loss	FAM188B INMT-FAM188B INMT
nsv436557	Chr.7:30288062 - 32730902 on Build GRCh38	Deletion	FAM188B MIR550A1 AVL9 ZNRF2P1 CCDC129 DKFZP586I1420 DPY19L1P1 GHRHR GGCT CRHR2 LINC01176 ZNRF2 GARS LOC401320 NEUROD6 MIR550B1 PDE1C AQP1 LOC101928268 LSM5 INMT-FAM188B ADCYAP1R1 LOC100130673 PPP1R17 INMT NOD1

More Information

• Set Membership: Intragenic, Non-exonic, DGV Variation