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          • › Hs04211858_cn
          See other FCGR3B CNV Assays ›
          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
          Price
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          • Genomic Map
          • Assay Details
          • More Information

          Genomic Map

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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 FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          esv2507888 Chr.1:161548423 - 161631182 on Build GRCh38 Deletion FCGR2C FCGR3B HSPA7 FCGR3A
          esv3325 Chr.1:161594843 - 161676929 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7
          esv5752 Chr.1:161594815 - 161676980 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7
          nsv517640 Chr.1:161525250 - 161692694 on Build GRCh38 Gain+Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A HSPA6 RPL31P11
          esv990743 Chr.1:161550050 - 161649676 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          esv2758972 Chr.1:161374465 - 161711762 on Build GRCh38 Gain+Loss FCGR2C FCGR2B FCGR3B FCRLA HSPA7 FCGR2A FCGR3A HSPA6 RPL31P11
          esv3587733 Chr.1:161600533 - 161628390 on Build GRCh38 Gain FCGR2C FCGR3B HSPA7
          nsv818500 Chr.1:161541303 - 161647726 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          dgv24n16 Chr.1:161571696 - 161671744 on Build GRCh38 Insertion FCGR2C FCGR2B FCGR3B HSPA7
          nsv548066 Chr.1:161587939 - 161647726 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7
          esv3584532 Chr.1:161541620 - 161669769 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          nsv548074 Chr.1:161623299 - 161671187 on Build GRCh38 Loss FCGR2B FCGR3B
          dgv605n54 Chr.1:161533359 - 161671187 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          esv28122 Chr.1:161439273 - 161676968 on Build GRCh38 Gain+Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          esv2670711 Chr.1:161620574 - 161628209 on Build GRCh38 Deletion FCGR3B
          nsv428257 Chr.1:161436525 - 161898473 on Build GRCh38 Loss FCGR2B HSPA7 FCRLB ATF6 DUSP12 LOC100422526 FCGR2C FCGR3B FCRLA FCGR2A FCGR3A HSPA6 RPL31P11
          nsv1161862 Chr.1:161539085 - 161678447 on Build GRCh38 Duplication FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          dgv606n54 Chr.1:161572474 - 161671187 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7
          nsv820341 Chr.1:161510055 - 161678358 on Build GRCh38 Duplication FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          dgv447n100 Chr.1:161506699 - 161700539 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6 RPL31P11
          dgv38e201 Chr.1:161558346 - 161653012 on Build GRCh38 Deletion FCGR2C FCGR2B FCGR3B HSPA7
          nsv946468 Chr.1:161594892 - 161670153 on Build GRCh38 Duplication FCGR2C FCGR2B FCGR3B HSPA7
          nsv825254 Chr.1:161607568 - 161649676 on Build GRCh38 Gain FCGR2B FCGR3B HSPA7
          dgv448n100 Chr.1:161527110 - 161668711 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          esv3541689 Chr.1:161579211 - 161675381 on Build GRCh38 Deletion FCGR2C FCGR2B FCGR3B HSPA7
          esv2718873 Chr.1:161512733 - 161631124 on Build GRCh38 Deletion FCGR2C FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          esv3587734 Chr.1:161620485 - 161628311 on Build GRCh38 Loss FCGR3B
          dgv23n16 Chr.1:161543533 - 161631305 on Build GRCh38 Insertion FCGR2C FCGR3B HSPA7 FCGR3A
          dgv4n68 Chr.1:161433240 - 161696942 on Build GRCh38 Gain+Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6 RPL31P11
          nsv464173 Chr.1:161509955 - 161677017 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          nsv8502 Chr.1:161507558 - 161676760 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          nsv821621 Chr.1:161553439 - 161667052 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7
          nsv509546 Chr.1:161543042 - 161684642 on Build GRCh38 Insertion FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A RPL31P11
          dgv451n100 Chr.1:161532055 - 161678819 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          esv997087 Chr.1:161513165 - 161676614 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          dgv85n67 Chr.1:161519583 - 161678358 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          esv33393 Chr.1:161508891 - 162110537 on Build GRCh38 Gain+Loss FCGR2B HSPA7 OLFML2B NOS1AP FCRLB ATF6 DUSP12 LOC100422526 FCGR2C FCGR3B FCRLA FCGR2A FCGR3A HSPA6 RPL31P11
          nsv514915 Chr.1:161539698 - 161676786 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7 FCGR3A
          nsv825242 Chr.1:161589306 - 161649676 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7
          nsv1009190 Chr.1:161623061 - 161649256 on Build GRCh38 Gain+Loss FCGR2B FCGR3B
          dgv5e203 Chr.1:161508746 - 161668740 on Build GRCh38 Gain+Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6
          dgv75e199 Chr.1:161561480 - 161661159 on Build GRCh38 Deletion FCGR2C FCGR2B FCGR3B HSPA7
          dgv8e55 Chr.1:161493708 - 161703892 on Build GRCh38 Gain FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6 RPL31P11
          esv3890693 Chr.1:161521106 - 161654964 on Build GRCh38 Loss FCGR2C FCGR2B FCGR3B HSPA7 FCGR2A FCGR3A HSPA6

          Back To Top

          More Information


          Set Membership:

          Intragenic Intronic Non-exonic DGV Variation

          Panther Classification:

          Molecular Function -

          immunoglobulin receptor superfamily

          Gene Ontology Categories:

          Function(s) Process(es)

          positive regulation of defense response to virus by host
          immune response
          mitophagy in response to mitochondrial depolarization
          xenophagy
          IgG binding

          Back To Top

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