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Variant : CV803322 (GRCh37/hg19 8p21.2-21.1(chr8:24305969-28673405)x1) Homo sapiens

Symbol: CV803322
Name: GRCh37/hg19 8p21.2-21.1(chr8:24305969-28673405)x1
Condition: not provided [RCV001006090]
Clinical Significance: pathogenic
Last Evaluated: 11/30/2018
Review Status: no assertion criteria provided
Related Genes: ADAM7   ADRA1A   BNIP3L   CCDC25   CDCA2   CHRNA2   CLU   DOCK5   DPYSL2   EBF2   ELP3   EPHX2   ESCO2   EXTL3   FBXO16   FZD3   GNRH1   INTS9   KCTD9   NEFL   NEFM   NUGGC   PBK   PNMA2   PNOC   PPP2R2A   PTK2B   SCARA3   SCARA5   STMN4   TRIM35   ZNF395  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37824,305,969 - 28,673,405CLINVAR
Cytogenetic Map88p21.2-21.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 25315753
Created: 2020-04-07
Species: Homo sapiens
Last Modified: 2020-06-23
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.