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Variant : CV676062 (GRCh37/hg19 8p21.3-21.2(chr8:21662847-24199218)x1) Homo sapiens

Symbol: CV676062
Name: GRCh37/hg19 8p21.3-21.2(chr8:21662847-24199218)x1
Condition: not provided [RCV000849161]
Clinical Significance: pathogenic
Last Evaluated: 04/18/2017
Review Status: no assertion criteria provided
Related Genes: ADAM28   BIN3   BMP1   C8orf58   CCAR2   CHMP7   DMTN   DOK2   EGR3   ENTPD4   FAM160B2   FGF17   HR   LGI3   LOXL2   MIR320A   NKX2-6   NKX3-1   NPM2   NUDT18   PDLIM2   PEBP4   PHYHIP   PIWIL2   POLR3D   PPP3CC   R3HCC1   REEP4   RHOBTB2   SFTPC   SLC25A37   SLC39A14   SORBS3   STC1   TNFRSF10A   TNFRSF10B   TNFRSF10C   TNFRSF10D   XPO7  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37821,662,847 - 24,199,218CLINVAR
Cytogenetic Map88p21.3-21.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980682
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-10-20
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.