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Variant : CV383869 (GRCh37/hg19 2q37.3(chr2:242416476-242783384)x1) Homo sapiens

Symbol: CV383869
Name: GRCh37/hg19 2q37.3(chr2:242416476-242783384)x1
Condition: See cases [RCV000446678]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ATG4B   BOK   D2HGDH   DTYMK   FARP2   GAL3ST2   ING5   NEU4   STK25   THAP4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372242,416,476 - 242,783,384CLINVAR
Cytogenetic Map22q37.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12851401
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-05-12
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.