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Variant : CV652378 (NC_000015.9:g.(?_30906589)_(31244241_?)del) Homo sapiens

Symbol: CV652378
Name: NC_000015.9:g.(?_30906589)_(31244241_?)del
Condition: not provided [RCV000823253]
Clinical Significance: pathogenic
Last Evaluated: 08/30/2018
Review Status: criteria provided, single submitter
Related Genes: ARHGAP11B   FAN1   GOLGA8H   MTMR10  
Variant Type: deletion (SO:0000159)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_30906589)_(31244241_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381530,614,386 - 30,952,038CLINVAR
GRCh371530,906,589 - 31,244,241CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14702296
Created: 2019-09-06
Species: Homo sapiens
Last Modified: 2019-10-08
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.