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Variant : CV673160 (GRCh37/hg19 14q11.2(chr14:20511672-21174548)x3) Homo sapiens

Symbol: CV673160
Name: GRCh37/hg19 14q11.2(chr14:20511672-21174548)x3
Condition: not provided [RCV000846276]
Clinical Significance: uncertain significance
Last Evaluated: 06/06/2017
Review Status: no assertion criteria provided
Related Genes: ANG   APEX1   CCNB1IP1   KLHL33   OR11G2   OR11H4   OR11H6   OR4K17   OR4L1   OR4N5   OR6S1   OSGEP   PARP2   PIP4P1   PNP   RNASE10   RNASE11   RNASE12   RNASE4   RNASE9   RPPH1   TEP1   TRL-AAG2-3   TRP-AGG2-5   TRP-AGG2-6   TRT-TGT3-1   TTC5  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371420,511,672 - 21,174,548CLINVAR
Cytogenetic Map1414q11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14981541
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE



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