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Variant : CV382797 (GRCh37/hg19 16p13.3(chr16:4541805-5813911)x3) Homo sapiens

Symbol: CV382797
Name: GRCh37/hg19 16p13.3(chr16:4541805-5813911)x3
Condition: See cases [RCV000448804]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ALG1   ANKS3   C16orf71   C16orf89   C16orf96   CDIP1   EEF2KMT   GLYR1   HMOX2   MGRN1   NAGPA   NUDT16L1   PPL   ROGDI   SEC14L5   SEPTIN12   SMIM22   UBALD1   UBN1   ZNF500  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37164,541,805 - 5,813,911CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853504
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-01-21
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.