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Variant : CV248177 (GRCh37/hg19 16p13.3(chr16:3104050-3722491)x3) Homo sapiens

Symbol: CV248177
Name: GRCh37/hg19 16p13.3(chr16:3104050-3722491)x3
Condition: See cases [RCV000240036]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: C16orf90   CLUAP1   DNASE1   IL32   MEFV   MMP25   MTRNR2L4   NAA60   NLRC3   OR1F1   OR2C1   SLX4   TIGD7   TRAP1   ZNF174   ZNF200   ZNF205   ZNF213   ZNF263   ZNF597   ZNF75A   ZSCAN10   ZSCAN32  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37163,104,050 - 3,722,491CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541502
Created: 2016-10-11
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.