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Variant : CV550798 (NC_000003.11:g.4134224_4909191dup) Homo sapiens

Symbol: CV550798
Name: NC_000003.11:g.4134224_4909191dup
Condition: not provided [RCV000677959]
Clinical Significance: uncertain significance
Last Evaluated: 05/01/2017
Review Status: criteria provided, single submitter
Related Genes: EGOT   ITPR1   SETMAR   SUMF1  
Variant Type: duplication (SO:1000035)
Evidence: provider interpretation
HGVS Name(s): NC_000003.11:g.4134224_4909191dup
Human AssemblyChrPosition (strand)Source
GRCh3734,134,224 - 4,909,191CLINVAR
Cytogenetic Map33p26.1CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13790584
Created: 2018-09-11
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.