Search
LOADING 
- Gene Symbol
- FCGR3B
- Assay Reference Genome
Location
Chr.1:161626930 on build GRCh38- Cytoband
- 1q23.3
Genomic Map
Back To TopAssay 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 TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top