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Variant : CV437175 (GRCh37/hg19 22q11.21-11.22(chr22:21029655-22481498)x1) Homo sapiens

Symbol: CV437175
Name: GRCh37/hg19 22q11.21-11.22(chr22:21029655-22481498)x1
Condition: See cases [RCV000511898]
Clinical Significance: uncertain significance
Last Evaluated: 06/03/2014
Review Status: no assertion criteria provided
Related Genes: AIFM3   CCDC116   CRKL   GGT2   HIC2   LZTR1   MAPK1   MIR130B   P2RX6   PI4KA   PPIL2   PPM1F   PPM1F-AS1   RIMBP3B   RIMBP3C   SDF2L1   SERPIND1   SLC7A4   SNAP29   THAP7   TMEM191C   TOP3B   UBE2L3   YDJC   YPEL1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372221,029,655 - 22,481,498CLINVAR
Cytogenetic Map2222q11.21-11.22CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444867
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-11-12
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.