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Variant : CV606270 (GRCh37/hg19 16p13.2(chr16:8828410-9028645)x3) Homo sapiens

Symbol: CV606270
Name: GRCh37/hg19 16p13.2(chr16:8828410-9028645)x3
Condition: not provided [RCV000751570]
Clinical Significance: benign
Last Evaluated: 12/04/2014
Review Status: no assertion criteria provided
Related Genes: ABAT   CARHSP1   PMM2   TMEM186   USP7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37168,828,410 - 9,028,645CLINVAR
Cytogenetic Map1616p13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366896
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-12
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.