Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Variant : CV675449 (GRCh37/hg19 16q12.2-21(chr16:53455650-64006604)x3) Homo sapiens

Symbol: CV675449
Name: GRCh37/hg19 16q12.2-21(chr16:53455650-64006604)x3
Condition: not provided [RCV000848548]
Clinical Significance: uncertain significance
Last Evaluated: 08/23/2018
Review Status: no assertion criteria provided
Related Genes: ADGRG1   ADGRG3   ADGRG5   AKTIP   AMFR   ARL2BP   BBS2   CAPNS2   CCDC102A   CCDC113   CCL17   CCL22   CDH8   CES1   CES5A   CETP   CFAP20   CIAPIN1   CNGB1   CNOT1   COQ9   CPNE2   CSNK2A2   CX3CL1   DOK4   DRC7   FTO   GINS3   GNAO1   GOT2   HERPUD1   IRX3   IRX5   IRX6   KATNB1   KIFC3   LPCAT2   MIR138-2   MMP15   MMP2   MT1A   MT1B   MT1E   MT1F   MT1G   MT1H   MT1M   MT1X   MT2A   MT3   MT4   NDRG4   NLRC5   NUDT21   NUP93   OGFOD1   PLLP   POLR2C   PRSS54   PSME3IP1   RBL2   RPGRIP1L   RSPRY1   SETD6   SLC12A3   SLC38A7   SLC6A2   TEPP   USB1   ZNF319  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371653,455,650 - 64,006,604CLINVAR
Cytogenetic Map1616q12.2-21CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14976546
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-11-05
Status: ACTIVE



NHLBI Logo

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