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Variant : CV554728 (GRCh37/hg19 8q11.1-11.23(chr8:46863521-55218838)x3) Homo sapiens

Symbol: CV554728
Name: GRCh37/hg19 8q11.1-11.23(chr8:46863521-55218838)x3
Condition: not provided [RCV000683033]
Clinical Significance: uncertain significance
Last Evaluated: 05/07/2018
Review Status: no assertion criteria provided
Related Genes: ALKAL1   ATP6V1H   CEBPD   EFCAB1   LINC00293   LYPLA1   MCM4   MRPL15   NPBWR1   OPRK1   PCMTD1   PPDPFL   PRKDC   PXDNL   RB1CC1   RGS20   SNAI2   SNTG1   SPIDR   ST18   TCEA1   UBE2V2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37846,863,521 - 55,218,838CLINVAR
Cytogenetic Map88q11.1-11.23CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 13795934
Created: 2018-10-09
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.