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Variant : CV384206 (GRCh37/hg19 3p26.1(chr3:4327821-4404525)x1) Homo sapiens

Symbol: CV384206
Name: GRCh37/hg19 3p26.1(chr3:4327821-4404525)x1
Condition: See cases [RCV000449247]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: SETMAR   SUMF1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3734,327,821 - 4,404,525CLINVAR
Cytogenetic Map33p26.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853943
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2019-12-03
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.