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Variant : CV437286 (GRCh37/hg19 8q21.11-21.13(chr8:77751515-83516216)x1) Homo sapiens

Symbol: CV437286
Name: GRCh37/hg19 8q21.11-21.13(chr8:77751515-83516216)x1
Condition: See cases [RCV000511429]
Clinical Significance: pathogenic
Last Evaluated: 11/12/2013
Review Status: no assertion criteria provided
Related Genes: CHMP4C   FABP12   FABP4   FABP5   FABP9   HEY1   IL7   IMPA1   MRPS28   PAG1   PEX2   PKIA   PMP2   SLC10A5   SNX16   STMN2   TPD52   ZBTB10   ZC2HC1A   ZFAND1   ZFHX4   ZNF704  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37877,751,515 - 83,516,216CLINVAR
Cytogenetic Map88q21.11-21.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13444401
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-01-14
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.