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Variant : CV161396 (GRCh38/hg38 16p13.3(chr16:534395-722554)x3) Homo sapiens

Symbol: CV161396
Name: GRCh38/hg38 16p13.3(chr16:534395-722554)x3
Condition: See cases [RCV000140349]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ANTKMT   CAPN15   FBXL16   JMJD8   MCRIP2   METRN   METTL26   MIR3176   MIR5587   NHLRC4   PIGQ   PRR35   RAB40C   RHBDL1   RHOT2   STUB1   TRG-CCC2-2   WDR24   WDR90   WFIKKN1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_534395)_(722554_?)dup
NC_000016.9:g.(?_584395)_(772554_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3816534,395 - 722,554CLINVAR
GRCh3716584,395 - 772,554CLINVAR
Build 3616524,396 - 712,555CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487879
Created: 2014-09-09
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.