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Variant : CV674595 (GRCh37/hg19 16q23.3(chr16:83838342-83941401)x1) Homo sapiens

Symbol: CV674595
Name: GRCh37/hg19 16q23.3(chr16:83838342-83941401)x1
Condition: not provided [RCV000847711]
Clinical Significance: uncertain significance
Last Evaluated: 07/28/2017
Review Status: no assertion criteria provided
Related Genes: HSBP1   MLYCD  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371683,838,342 - 83,941,401CLINVAR
Cytogenetic Map1616q23.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979195
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.