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Variant : CV382614 (GRCh37/hg19 8p21.2-12(chr8:24514488-34808438)) Homo sapiens

Symbol: CV382614
Name: GRCh37/hg19 8p21.2-12(chr8:24514488-34808438)
Condition: See cases [RCV000448582]
Clinical Significance: pathogenic
Last Evaluated: 04/30/2011
Review Status: no assertion criteria provided
Related Genes: ADRA1A   BNIP3L   CCDC25   CDCA2   CHRNA2   CLU   DCTN6   DOCK5   DPYSL2   DUSP26   DUSP4   EBF2   ELP3   EPHX2   ESCO2   EXTL3   FBXO16   FUT10   FZD3   GNRH1   GSR   GTF2E2   HMBOX1   INTS9   KCTD9   KIF13B   LEPROTL1   MAK16   MBOAT4   NEFL   NEFM   NRG1   NUGGC   PBK   PNMA2   PNOC   PPP2CB   PPP2R2A   PTK2B   PURG   RBPMS   RNF122   SARAF   SCARA3   SCARA5   SMIM18   STMN4   TEX15   TRIM35   TTI2   UBXN8   WRN   ZNF395  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37824,514,488 - 34,808,438CLINVAR
Cytogenetic Map88p21.2-12CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853288
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-03-31
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.