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Variant : CV650587 (NC_000001.11:g.(?_43446935)_(43450500_?)del) Homo sapiens

Symbol: CV650587
Name: NC_000001.11:g.(?_43446935)_(43450500_?)del
Condition: not provided [RCV000815275]
Clinical Significance: uncertain significance
Last Evaluated: 11/13/2018
Review Status: criteria provided, single submitter
Related Genes: MIR6735   SZT2   SZT2-AS1  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000001.10:g.(?_43912606)_(43916171_?)del
NC_000001.11:g.(?_43446935)_(43450500_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38143,446,935 - 43,450,500CLINVAR
GRCh37143,912,606 - 43,916,171CLINVAR
Cytogenetic Map11p34.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14701281
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2020-07-28
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.