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Variant : CV555444 (GRCh37/hg19 16p13.3(chr16:3519135-3651271)x1) Homo sapiens

Symbol: CV555444
Name: GRCh37/hg19 16p13.3(chr16:3519135-3651271)x1
Condition: not provided [RCV000683749]
Clinical Significance: uncertain significance
Last Evaluated: 11/21/2017
Review Status: no assertion criteria provided
Related Genes: C16orf90   CLUAP1   NAA60   NLRC3   SLX4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37163,519,135 - 3,651,271CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13797552
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.