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Variant : CV556395 (GRCh37/hg19 1q32.1(chr1:200873507-201947585)x3) Homo sapiens

Symbol: CV556395
Name: GRCh37/hg19 1q32.1(chr1:200873507-201947585)x3
Condition: not provided [RCV000684686]
Clinical Significance: uncertain significance
Last Evaluated: 09/13/2017
Review Status: no assertion criteria provided
Related Genes: ASCL5   CACNA1S   CSRP1   IGFN1   INAVA   IPO9   KIF21B   LAD1   LMOD1   NAV1   PHLDA3   PKP1   SHISA4   TIMM17A   TMEM9   TNNI1   TNNT2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371200,873,507 - 201,947,585CLINVAR
Cytogenetic Map11q32.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798928
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-19
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.