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Variant : CV676434 (GRCh37/hg19 16q23.3(chr16:83830451-83948495)x1) Homo sapiens

Symbol: CV676434
Name: GRCh37/hg19 16q23.3(chr16:83830451-83948495)x1
Condition: not provided [RCV000849533]
Clinical Significance: uncertain significance
Last Evaluated: 12/01/2017
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
GRCh371683,830,451 - 83,948,495CLINVAR
Cytogenetic Map1616q23.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14981044
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.