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Gene Symbol
FCGR3B
Assay Reference Genome
Location

Chr.1:161626930 on build GRCh38
Cytoband
1q23.3
Assay ID Hs04211858_cn
Size
Availability Made To Order
Catalog # 4400291
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Assay Details

Target Gene Details

Entrez Gene ID:

 2215

Gene Name:

 Fc fragment of IgG receptor IIIb

Gene Aliases:

 CD16, CD16b, FCG3, FCGR3, FCR-10, FCRIII, FCRIIIb

Location:

 Chr.1:161623196-161631963 on Build GRCh38

Assay Gene Location:

 Within Intron 5
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
FCGR3B NM_000570.4 NP_000561.3
NM_001244753.1 NP_001231682.1
NM_001271035.1 NP_001257964.1
NM_001271036.1 NP_001257965.1
NM_001271037.1 NP_001257966.1
AB025256.1 BAA83803.1
AJ581669.1 CAE46408.1
AK313219.1
AK316565.1
BC128562.1
DA669913.1
DA670720.1
DA671001.1
DA672751.1
DA673839.1
J04162.1 AAA35881.1
M24854.1 AAA53507.1
X07934.1 CAA30758.1
X16863.1 CAA34753.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
nsv819523 Chr.1:161521768 - 161662864 on Build GRCh38 Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
esv2507888 Chr.1:161548423 - 161631182 on Build GRCh38 Deletion HSPA7 FCGR3B FCGR3A FCGR2C
esv3325 Chr.1:161594843 - 161676929 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR2C
esv5752 Chr.1:161594815 - 161676980 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR2C
nsv818489 Chr.1:161525250 - 161677034 on Build GRCh38 Gain FCGR2B HSPA7 HSPA6 FCGR3B FCGR3A FCGR2C
esv2758972 Chr.1:161374465 - 161711762 on Build GRCh38 Gain+Loss RPL31P11 FCGR2B HSPA7 HSPA6 FCRLA FCGR2A FCGR3B FCGR3A FCGR2C
esv990743 Chr.1:161550050 - 161649676 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
esv3587732 Chr.1:161600533 - 161628390 on Build GRCh38 Loss HSPA7 FCGR3B FCGR2C
dgv607n54 Chr.1:161587939 - 161661908 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR2C
dgv24n16 Chr.1:161571696 - 161671744 on Build GRCh38 Insertion FCGR2B HSPA7 FCGR3B FCGR2C
nsv818500 Chr.1:161541303 - 161647726 on Build GRCh38 Gain FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
nsv548074 Chr.1:161623299 - 161671187 on Build GRCh38 Loss FCGR2B FCGR3B
nsv442209 Chr.1:161541620 - 161669769 on Build GRCh38 Gain FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
esv28122 Chr.1:161439273 - 161676968 on Build GRCh38 Gain+Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
dgv605n54 Chr.1:161533359 - 161671187 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
nsv428257 Chr.1:161436525 - 161898473 on Build GRCh38 Loss HSPA6 FCRLA LOC100422526 FCGR2A FCGR3B FCRLB RPL31P11 FCGR2B HSPA7 ATF6 DUSP12 FCGR3A FCGR2C
esv2670711 Chr.1:161620574 - 161628209 on Build GRCh38 Deletion FCGR3B
dgv606n54 Chr.1:161572474 - 161671187 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR2C
nsv1161862 Chr.1:161539085 - 161678447 on Build GRCh38 Duplication FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
nsv825176 Chr.1:161510055 - 161677088 on Build GRCh38 Gain FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
dgv447n100 Chr.1:161506699 - 161700539 on Build GRCh38 Gain RPL31P11 FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
dgv38e201 Chr.1:161558346 - 161653012 on Build GRCh38 Deletion FCGR2B HSPA7 FCGR3B FCGR2C
nsv946468 Chr.1:161594892 - 161670153 on Build GRCh38 Duplication FCGR2B HSPA7 FCGR3B FCGR2C
nsv825254 Chr.1:161607568 - 161649676 on Build GRCh38 Gain FCGR2B HSPA7 FCGR3B
dgv449n100 Chr.1:161527110 - 161682500 on Build GRCh38 Gain+Loss FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
esv2718873 Chr.1:161512733 - 161631124 on Build GRCh38 Deletion HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
esv3541689 Chr.1:161579211 - 161675381 on Build GRCh38 Deletion FCGR2B HSPA7 FCGR3B FCGR2C
esv3587734 Chr.1:161620485 - 161628311 on Build GRCh38 Loss FCGR3B
dgv23n16 Chr.1:161543533 - 161631305 on Build GRCh38 Insertion HSPA7 FCGR3B FCGR3A FCGR2C
nsv519779 Chr.1:161509955 - 161668596 on Build GRCh38 Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
dgv4n68 Chr.1:161433240 - 161696942 on Build GRCh38 Gain+Loss RPL31P11 FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
nsv8502 Chr.1:161507558 - 161676760 on Build GRCh38 Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
nsv821621 Chr.1:161553439 - 161667052 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR2C
nsv509546 Chr.1:161543042 - 161684642 on Build GRCh38 Insertion RPL31P11 FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
dgv85n67 Chr.1:161519583 - 161678358 on Build GRCh38 Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
esv997087 Chr.1:161513165 - 161676614 on Build GRCh38 Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
dgv450n100 Chr.1:161532055 - 161668399 on Build GRCh38 Gain FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
esv33393 Chr.1:161508891 - 162110537 on Build GRCh38 Gain+Loss HSPA6 FCRLA NOS1AP LOC100422526 FCGR2A OLFML2B FCGR3B FCRLB RPL31P11 FCGR2B HSPA7 ATF6 DUSP12 FCGR3A FCGR2C
nsv1014271 Chr.1:161623061 - 161668066 on Build GRCh38 Loss FCGR2B FCGR3B
nsv825242 Chr.1:161589306 - 161649676 on Build GRCh38 Loss FCGR2B HSPA7 FCGR3B FCGR2C
nsv514915 Chr.1:161539698 - 161676786 on Build GRCh38 Gain FCGR2B HSPA7 FCGR3B FCGR3A FCGR2C
dgv5e203 Chr.1:161508746 - 161668740 on Build GRCh38 Gain+Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
dgv75e199 Chr.1:161561480 - 161661159 on Build GRCh38 Deletion FCGR2B HSPA7 FCGR3B FCGR2C
dgv8e55 Chr.1:161493708 - 161703892 on Build GRCh38 Gain RPL31P11 FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C
esv3890693 Chr.1:161521106 - 161654964 on Build GRCh38 Loss FCGR2B HSPA7 HSPA6 FCGR2A FCGR3B FCGR3A FCGR2C

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More Information


Set Membership:

 Intragenic Intronic Non-exonic DGV Variation

Panther Classification:

Gene Ontology Categories:

Function(s) Process(es)


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