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Variant : CV165396 (GRCh38/hg38 16p13.3(chr16:35880-605262)x1) Homo sapiens

Symbol: CV165396
Name: GRCh38/hg38 16p13.3(chr16:35880-605262)x1
Condition: See cases [RCV000143709]
Clinical Significance: uncertain significance
Last Evaluated: 03/10/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARHGDIG   AXIN1   CAPN15   DECR2   FAM234A   HBA1   HBA2   HBM   HBQ1   HBZ   LINC00235   LUC7L   MIR3176   MIR5587   MPG   MRPL28   NHLRC4   NME4   NPRL3   PDIA2   PGAP6   PIGQ   POLR3K   PRR35   RAB11FIP3   RAB40C   RGS11   RHBDF1   SNRNP25  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_35880)_(605262_?)del
NC_000016.9:g.(?_85880)_(655262_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381635,880 - 605,262CLINVAR
GRCh371685,880 - 655,262CLINVAR
Build 361625,880 - 595,263CLINVAR
Cytogenetic Map1616p13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9491307
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.