Hs03417857_cn

• Gene Symbol: FAM178B
• Assay Reference Genome Location: Chr.2:96919679 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 13

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

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 Intron 1

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

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

More Information

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