Hs03444416_cn

• Gene Symbol: FAM178B
• Assay Reference Genome Location: Chr.2:96924304 on build GRCh38
• Cytoband: 2q11.2

Target Gene Details

• Entrez Gene ID: 51252
• Gene Name: family with sequence similarity 178 member B
• Gene Aliases: -
• Location: Chr.2:96875882-96986600 on Build GRCh38
• Assay Gene Location: Within Intron 10

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FAM178B	NM_001122646.2			NP_001116118.2
	XM_011511294.2			XP_011509596.1
	XM_017004263.1			XP_016859752.1
	XM_017004264.1			XP_016859753.1
	XM_017004265.1			XP_016859754.1
	XM_017004266.1			XP_016859755.1
	AK122705.1
	AK308698.1
	BC039488.1			AAH39488.1
	DA357118.1

Target Gene Details

• Entrez Gene ID: 101927053
• Gene Name: uncharacterized LOC101927053
• Gene Aliases: -
• Location: Chr.2:96919106-96925837 on Build GRCh38
• Assay Gene Location: Within Exon 3

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
LOC101927053	NR_110209.1	3	727

Target Copy Number Variation Details

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

Target Variation	Location	CNV Subtype	Genes
nsv582497	Chr.2:96903568 - 97049417 on Build GRCh38	Loss	FAM178B LOC101927053
nsv526313	Chr.2:96667755 - 96994882 on Build GRCh38	Loss	FAM178B LMAN2L ANKRD23 ANKRD39 LOC101927053 FER1L5 SEMA4C CNNM4 CNNM3 MIR3127
dgv607e201	Chr.2:95855884 - 97561622 on Build GRCh38	Deletion	DUSP2 LOC100506123 LOC101927053 LOC107984110 ASTL STARD7 ANKRD36C FAM178B ANKRD36B ANKRD23 FER1L5 KANSL3 LOC105373495 FAHD2B GPAT2 LOC105373496 ANKRD36 ANKRD39 LOC100506076 FAHD2CP CNNM4 STARD7-AS1 NCAPH SNRNP200 MIR3127 ARID5A ITPRIPL1 LMAN2L ADRA2B SEMA4C NEURL3 CIAO1 LOC653924 TMEM127 CNNM3
nsv1135873	Chr.2:95981454 - 97579645 on Build GRCh38	Deletion	DUSP2 LOC100506123 LOC101927053 LOC107984110 ASTL STARD7 ANKRD36C FAM178B ANKRD36B ANKRD23 FER1L5 KANSL3 LOC105373495 FAHD2B GPAT2 LOC105373496 ANKRD36 ANKRD39 LOC100506076 FAHD2CP CNNM4 STARD7-AS1 NCAPH SNRNP200 MIR3127 ARID5A ITPRIPL1 LMAN2L ADRA2B SEMA4C NEURL3 CIAO1 LOC653924 TMEM127 CNNM3
esv2759077	Chr.2:96905372 - 97720044 on Build GRCh38	Gain+Loss	FAHD2B FAM178B ANKRD36B LOC100506123 ANKRD36 COX5B LOC101927053 LINC01125 LOC100506076 ZAP70 ACTR1B LOC653924
esv3425717	Chr.2:95859900 - 97515905 on Build GRCh38	Duplication	DUSP2 LOC100506123 LOC101927053 LOC107984110 ASTL STARD7 ANKRD36C FAM178B ANKRD36B ANKRD23 FER1L5 KANSL3 LOC105373495 FAHD2B GPAT2 LOC105373496 ANKRD36 ANKRD39 LOC100506076 FAHD2CP CNNM4 STARD7-AS1 NCAPH SNRNP200 MIR3127 ARID5A ITPRIPL1 LMAN2L ADRA2B SEMA4C NEURL3 CIAO1 LOC653924 TMEM127 CNNM3

More Information

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