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Variant : CV820975 (NC_000016.9:g.(?_624055)_(2550979_?)dup) Homo sapiens

Symbol: CV820975
Name: NC_000016.9:g.(?_624055)_(2550979_?)dup
Condition: Idiopathic generalized epilepsy [RCV001033790]
Clinical Significance: uncertain significance
Last Evaluated: 08/14/2019
Review Status: criteria provided, single submitter
Related Genes: ABCA3   ANTKMT   BAIAP3   BRICD5   C16orf91   C1QTNF8   CACNA1H   CASKIN1   CCDC154   CCDC78   CCNF   CHTF18   CIAO3   CLCN7   CRAMP1   DNASE1L2   E4F1   ECI1   EME2   FAHD1   FBXL16   GFER   GNG13   GNPTG   HAGH   HAGHL   HS3ST6   IFT140   IGFALS   JMJD8   JPT2   LMF1   MAPK8IP3   MCRIP2   MEIOB   METRN   METTL26   MIR1225   MLST8   MRPS34   MSLN   MSRB1   NDUFB10   NME3   NOXO1   NPW   NTHL1   NTN3   NUBP2   PGP   PIGQ   PKD1   PRR25   PTX4   RAB26   RAB40C   RHBDL1   RHOT2   RNF151   RNPS1   RPL3L   RPS2   RPUSD1   SLC9A3R2   SNHG9   SOX8   SPSB3   SSTR5   STUB1   SYNGR3   TBC1D24   TBL3   TEDC2   TELO2   TMEM204   TPSAB1   TPSB2   TPSD1   TPSG1   TRAF7   TSC2   TSR3   UBE2I   UNKL   WDR24   WDR90   WFIKKN1   ZNF598  
Variant Type: duplication (SO:1000035)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.9:g.(?_624055)_(2550979_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3716624,055 - 2,550,979CLINVAR
Cytogenetic Map1616p13.3CLINVAR
Trait Synonyms: ALDOSTERONISM, PRIMARY, AND HYPERTENSION; EIG; FH IV; Hyperaldosteronism, familial, type IV



Disease Annotations
References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 26898686
Created: 2020-05-12
Species: Homo sapiens
Last Modified: 2020-10-15
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.