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Variant : CV434721 (GRCh37/hg19 22q11.23-12.1(chr22:24652837-25970705)x3) Homo sapiens

Symbol: CV434721
Name: GRCh37/hg19 22q11.23-12.1(chr22:24652837-25970705)x3
Condition: not provided [RCV000509448]
Clinical Significance: not provided
Last Evaluated:
Review Status: no assertion provided
Related Genes: ADORA2A   CRYBB2   CRYBB3   GGT1   GRK3   GUCD1   KIAA1671   LRP5L   LRRC75B   PIWIL3   SGSM1   SNRPD3   SPECC1L   TMEM211   UPB1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: phenotyping only
Position
Human AssemblyChrPosition (strand)Source
GRCh372224,652,837 - 25,970,705CLINVAR
Cytogenetic Map2222q11.23-12.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13442605
Created: 2017-11-07
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.