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Variant : CV554960 (GRCh37/hg19 10q26.3(chr10:133574560-135296619)x4) Homo sapiens

Symbol: CV554960
Name: GRCh37/hg19 10q26.3(chr10:133574560-135296619)x4
Condition: not provided [RCV000683265]
Clinical Significance: uncertain significance
Last Evaluated: 08/24/2017
Review Status: no assertion criteria provided
Related Genes: ADAM8   ADGRA1   BNIP3   CALY   CFAP46   DPYSL4   ECHS1   FUOM   INPP5A   JAKMIP3   KNDC1   LINC01166   LINC02870   LRRC27   MTG1   NKX6-2   PAOX   PPP2R2D   PRAP1   PWWP2B   SPRN   STK32C   TUBGCP2   UTF1   VENTX   ZNF511  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710133,574,560 - 135,296,619CLINVAR
Cytogenetic Map1010q26.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796310
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-05-26
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.