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Variant : CV437247 (GRCh37/hg19 2q37.3(chr2:241997911-242783384)x3) Homo sapiens

Symbol: CV437247
Name: GRCh37/hg19 2q37.3(chr2:241997911-242783384)x3
Condition: See cases [RCV000512463]
Clinical Significance: uncertain significance
Last Evaluated: 02/01/2016
Review Status: no assertion criteria provided
Related Genes: ANO7   ATG4B   BOK   D2HGDH   DTYMK   FARP2   GAL3ST2   HDLBP   ING5   MTERF4   NEU4   PASK   PPP1R7   SEPTIN2   SNED1   STK25   THAP4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372241,997,911 - 242,783,384CLINVAR
Cytogenetic Map22q37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445425
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-12-03
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.