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See other FAM178B CNV Assays ›
Gene Symbol
FAM178B
Assay Reference Genome
Location

Chr.2:96876326 on build GRCh38
Cytoband
2q11.2
Assay ID Hs02369694_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

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 21 - Exon 22
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FAM178B NM_001122646.2 NP_001116118.2
NM_001172667.1 NP_001166138.1
NM_016490.4 NP_057574.2
XM_011511294.2 XP_011509596.1
XM_017004263.1 XP_016859752.1
XM_017004264.1 XP_016859753.1
XM_017004266.1 XP_016859755.1
XM_017004267.1 XP_016859756.1
XM_017004268.1 XP_016859757.1
AF151068.1 AAF36154.1
AJ710728.1
AK122705.1
AK308698.1
BC038583.1 AAH38583.3
BC039488.1 AAH39488.1
BC051379.1 AAH51379.1
BX103404.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv526313 Chr.2:96667755 - 96994882 on Build GRCh38 Loss MIR3127 LOC101927053 SEMA4C FAM178B LMAN2L CNNM3 ANKRD23 FER1L5 ANKRD39 CNNM4
dgv607e201 Chr.2:95855884 - 97561622 on Build GRCh38 Deletion ADRA2B TMEM127 STARD7-AS1 SEMA4C NEURL3 ANKRD39 ANKRD36C LOC653924 ARID5A FAM178B STARD7 FER1L5 LOC100506076 KANSL3 CNNM4 LOC105373495 MIR3127 FAHD2CP NCAPH LMAN2L CNNM3 SNRNP200 ANKRD36 CIAO1 DUSP2 LOC107984110 ITPRIPL1 ANKRD36B GPAT2 LOC105373496 LOC101927053 FAHD2B ASTL LOC100506123 ANKRD23
nsv1135873 Chr.2:95981454 - 97579645 on Build GRCh38 Deletion ADRA2B TMEM127 STARD7-AS1 SEMA4C NEURL3 ANKRD39 ANKRD36C LOC653924 ARID5A FAM178B STARD7 FER1L5 LOC100506076 KANSL3 CNNM4 LOC105373495 MIR3127 FAHD2CP NCAPH LMAN2L CNNM3 SNRNP200 ANKRD36 CIAO1 DUSP2 LOC107984110 ITPRIPL1 ANKRD36B GPAT2 LOC105373496 LOC101927053 FAHD2B ASTL LOC100506123 ANKRD23
esv3425717 Chr.2:95859900 - 97515905 on Build GRCh38 Duplication ADRA2B TMEM127 STARD7-AS1 SEMA4C NEURL3 ANKRD39 ANKRD36C LOC653924 ARID5A FAM178B STARD7 FER1L5 LOC100506076 KANSL3 CNNM4 LOC105373495 MIR3127 FAHD2CP NCAPH LMAN2L CNNM3 SNRNP200 ANKRD36 CIAO1 DUSP2 LOC107984110 ITPRIPL1 ANKRD36B GPAT2 LOC105373496 LOC101927053 FAHD2B ASTL LOC100506123 ANKRD23

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More Information


Set Membership:

 Intragenic Non-exonic DGV Variation

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