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Variant : CV381529 (GRCh37/hg19 2q37.3(chr2:242045569-243040217)x1) Homo sapiens

Symbol: CV381529
Name: GRCh37/hg19 2q37.3(chr2:242045569-243040217)x1
Condition: See cases [RCV000448540]
Clinical Significance: likely pathogenic
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ANO7   ATG4B   BOK   D2HGDH   DTYMK   FARP2   GAL3ST2   HDLBP   ING5   NEU4   PASK   PDCD1   PPP1R7   RTP5   SEPTIN2   STK25   THAP4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372242,045,569 - 243,040,217CLINVAR
Cytogenetic Map22q37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853247
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-20
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.