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Variant : CV162668 (GRCh38/hg38 8p23.3-22(chr8:226452-16280146)x3) Homo sapiens

Symbol: CV162668
Name: GRCh38/hg38 8p23.3-22(chr8:226452-16280146)x3
Condition: See cases [RCV000141418]
Clinical Significance: pathogenic
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AC016065.1   AC019257.1   AC022784.1   AC022832.2   AC068587.4   AC100797.5   AC100810.1   AC104964.1   AC105001.1   AC123777.1   AC246817.1   AF067845.2   AF131215.3   AF131216.3   AF233439.1   AGPAT5   ANGPT2   ARHGEF10   BLK   C8orf48   C8orf49   C8orf74   CLDN23   CLN8   CSMD1   CTSB   DEFA1   DEFA1B   DEFA3   DEFA4   DEFA5   DEFA6   DEFB1   DEFB103A   DEFB103B   DEFB104A   DEFB104B   DEFB105A   DEFB105B   DEFB106A   DEFB106B   DEFB107A   DEFB107B   DEFB109B   DEFB130A   DEFB130B   DEFB134   DEFB135   DEFB136   DEFB4A   DEFB4B   DLC1   DLGAP2   DLGAP2-AS1   ERI1   ERICH1   FAM167A   FAM167A-AS1   FAM66A   FAM66B   FAM66D   FAM66E   FAM85A   FAM85B   FAM86B1   FAM86B2   FAM87A   FBXO25   FDFT1   GATA4   KBTBD11   KBTBD11-OT1   LINC00208   LINC00681   LINC00965   LONRF1   MCPH1   MCPH1-AS1   MFHAS1   MIR124-1   MIR124-1HG   MIR1322   MIR3674   MIR383   MIR3926-1   MIR3926-2   MIR4286   MIR4659A   MIR4659B   MIR4660   MIR548I3   MIR5692A2   MIR596   MIR597   MIR598   MIR7160   MIR8055   MSR1   MSRA   MTMR9   MYOM2   NEIL2   PINX1   PPP1R3B   PRAG1   PRR23D1   PRR23D2   PRSS51   PRSS55   RP1L1   SGCZ   SLC35G5   SNORA99   SNORD3I   SOX7   SPAG11A   SPAG11B   TDRP   TNKS   TRMT9B   TUSC3   USP17L1   USP17L2   USP17L3   USP17L4   USP17L7   USP17L8   XKR5   XKR6   ZNF596   ZNF705B   ZNF705D   ZNF705G  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_226452)_(16280146_?)dup
Human AssemblyChrPosition (strand)Source
GRCh388226,452 - 16,280,146CLINVAR
GRCh378176,452 - 16,137,655CLINVAR
Build 368166,452 - 16,182,026CLINVAR
Cytogenetic Map88p23.3-22CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 9488943
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-06-23
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.