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Variant : CV803631 (GRCh37/hg19 11p14.1(chr11:28055151-28348275)x1) Homo sapiens

Symbol: CV803631
Name: GRCh37/hg19 11p14.1(chr11:28055151-28348275)x1
Condition: not provided [RCV001006399]
Clinical Significance: uncertain significance
Last Evaluated: 04/09/2019
Review Status: no assertion criteria provided
Related Genes: KIF18A   METTL15   MIR610  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371128,055,151 - 28,348,275CLINVAR
Cytogenetic Map1111p14.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25316198
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-09-08
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.