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Variant : CV675955 (GRCh37/hg19 16p13.3(chr16:2716924-3055626)x3) Homo sapiens

Symbol: CV675955
Name: GRCh37/hg19 16p13.3(chr16:2716924-3055626)x3
Condition: not provided [RCV000849054]
Clinical Significance: uncertain significance
Last Evaluated: 01/19/2018
Review Status: no assertion criteria provided
Related Genes: ELOB   FLYWCH1   FLYWCH2   KCTD5   KREMEN2   PAQR4   PKMYT1   PRSS21   PRSS22   PRSS27   PRSS33   PRSS41   SRRM2   ZG16B  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37162,716,924 - 3,055,626CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980580
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-03-17
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.