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Variant : CV676772 (GRCh37/hg19 14q11.2(chr14:21490055-21962265)x3) Homo sapiens

Symbol: CV676772
Name: GRCh37/hg19 14q11.2(chr14:21490055-21962265)x3
Condition: not provided [RCV000849871]
Clinical Significance: uncertain significance
Last Evaluated: 10/13/2017
Review Status: no assertion criteria provided
Related Genes: ARHGEF40   CHD8   HNRNPC   NDRG2   OR5AU1   RAB2B   RNASE13   RNASE7   RNASE8   RPGRIP1   SUPT16H   TMEM253   TOX4   TPPP2   ZNF219  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371421,490,055 - 21,962,265CLINVAR
Cytogenetic Map1414q11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14981363
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
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.