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Variant : CV675289 (GRCh37/hg19 3p26.1(chr3:4276014-4643555)x1) Homo sapiens

Symbol: CV675289
Name: GRCh37/hg19 3p26.1(chr3:4276014-4643555)x1
Condition: not provided [RCV000848388]
Clinical Significance: pathogenic
Last Evaluated: 12/06/2017
Review Status: no assertion criteria provided
Related Genes: ITPR1   SETMAR   SUMF1  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh3734,276,014 - 4,643,555CLINVAR
Cytogenetic Map33p26.1CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 14979945
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.