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Variant : CV625918 (GRCh37/hg19 22q13.1(chr22:38838246-39260032)x1) Homo sapiens

Symbol: CV625918
Name: GRCh37/hg19 22q13.1(chr22:38838246-39260032)x1
Condition: See cases [RCV000790565]
Clinical Significance: uncertain significance
Last Evaluated: 07/16/2018
Review Status: criteria provided, single submitter
Related Genes: CBY1   DDX17   DMC1   DNAL4   FAM227A   GTPBP1   JOSD1   KCNJ4   KDELR3   NPTXR   SUN2   TOMM22  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372238,838,246 - 39,260,032CLINVAR
Cytogenetic Map2222q13.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14697824
Created: 2019-08-06
Species: Homo sapiens
Last Modified: 2020-09-22
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.