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Variant : CV436397 (GRCh37/hg19 16p13.3(chr16:2606710-3382546)x3) Homo sapiens

Symbol: CV436397
Name: GRCh37/hg19 16p13.3(chr16:2606710-3382546)x3
Condition: See cases [RCV000512346]
Clinical Significance: uncertain significance
Last Evaluated: 12/14/2014
Review Status: no assertion criteria provided
Related Genes: BICDL2   CLDN6   CLDN9   ELOB   FLYWCH1   FLYWCH2   HCFC1R1   IL32   KCTD5   KREMEN2   MEFV   MMP25   OR1F1   PAQR4   PDPK1   PKMYT1   PRSS21   PRSS22   PRSS27   PRSS33   PRSS41   SRRM2   THOC6   TIGD7   TNFRSF12A   ZG16B   ZNF200   ZNF205   ZNF213   ZNF263   ZNF75A   ZSCAN10  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37162,606,710 - 3,382,546CLINVAR
Cytogenetic Map1616p13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13463034
Created: 2017-12-12
Species: Homo sapiens
Last Modified: 2020-03-31
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.