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Variant : CV435302 (GRCh37/hg19 14q32.12-32.13(chr14:93498930-96059698)x3) Homo sapiens

Symbol: CV435302
Name: GRCh37/hg19 14q32.12-32.13(chr14:93498930-96059698)x3
Condition: See cases [RCV000511246]
Clinical Significance: uncertain significance
Last Evaluated: 08/01/2014
Review Status: no assertion criteria provided
Related Genes: ASB2   BTBD7   CLMN   COX8C   DDX24   DICER1   FAM181A   GLRX5   GON7   GSC   IFI27   IFI27L1   IFI27L2   ITPK1   MOAP1   OTUB2   PPP4R4   PRIMA1   SERPINA1   SERPINA10   SERPINA11   SERPINA12   SERPINA2   SERPINA3   SERPINA4   SERPINA5   SERPINA6   SERPINA9   SNHG10   SYNE3   TMEM251   UBR7   UNC79  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371493,498,930 - 96,059,698CLINVAR
Cytogenetic Map1414q32.12-32.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444221
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.