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Variant : CV675564 (GRCh37/hg19 3q13.33-21.1(chr3:121384741-123672180)x3) Homo sapiens

Symbol: CV675564
Name: GRCh37/hg19 3q13.33-21.1(chr3:121384741-123672180)x3
Condition: not provided [RCV000848663]
Clinical Significance: uncertain significance
Last Evaluated: 03/21/2018
Review Status: no assertion criteria provided
Related Genes: ADCY5   CASR   CCDC14   CCDC58   CD86   CSTA   DTX3L   EAF2   FAM162A   GOLGB1   HACD2   HSPBAP1   ILDR1   IQCB1   KPNA1   MYLK   PARP14   PARP15   PARP9   PDIA5   SEC22A   SEMA5B   SLC15A2   SLC49A4   WDR5B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh373121,384,741 - 123,672,180CLINVAR
Cytogenetic Map33q13.33-21.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980207
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-02-20
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.