Hs03437924_cn

• Gene Symbol: FAM178B
• Assay Reference Genome Location: Chr.2:96921231 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: Overlaps Intron 12 - Exon 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 2

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

More Information

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