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Variant : CV672739 (GRCh37/hg19 3p26.1(chr3:4294669-4785230)x3) Homo sapiens

Symbol: CV672739
Name: GRCh37/hg19 3p26.1(chr3:4294669-4785230)x3
Condition: not provided [RCV000845855]
Clinical Significance: uncertain significance
Last Evaluated: 12/19/2017
Review Status: no assertion criteria provided
Related Genes: ITPR1   SETMAR   SUMF1  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3734,294,669 - 4,785,230CLINVAR
Cytogenetic Map33p26.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14976325
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE


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