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Variant : CV555650 (GRCh37/hg19 17q24.3(chr17:67131934-67321879)x3) Homo sapiens

Symbol: CV555650
Name: GRCh37/hg19 17q24.3(chr17:67131934-67321879)x3
Condition: not provided [RCV000683955]
Clinical Significance: uncertain significance
Last Evaluated: 02/21/2018
Review Status: no assertion criteria provided
Related Genes: ABCA10   ABCA5   ABCA6  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371767,131,934 - 67,321,879CLINVAR
Cytogenetic Map1717q24.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13798087
Created: 2018-10-09
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.