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Variant : CV555443 (GRCh37/hg19 16p13.3(chr16:3265427-3731182)x3) Homo sapiens

Symbol: CV555443
Name: GRCh37/hg19 16p13.3(chr16:3265427-3731182)x3
Condition: not provided [RCV000683748]
Clinical Significance: uncertain significance
Last Evaluated: 06/21/2017
Review Status: no assertion criteria provided
Related Genes: C16orf90   CLUAP1   DNASE1   MEFV   MTRNR2L4   NAA60   NLRC3   OR2C1   SLX4   TIGD7   TRAP1   ZNF174   ZNF200   ZNF263   ZNF597   ZNF75A   ZSCAN32  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37163,265,427 - 3,731,182CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13797549
Created: 2018-10-09
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.