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Variant : CV606433 (GRCh37/hg19 16q22.2(chr16:71697752-72032231)x1) Homo sapiens

Symbol: CV606433
Name: GRCh37/hg19 16q22.2(chr16:71697752-72032231)x1
Condition: not provided [RCV000751733]
Clinical Significance: benign
Last Evaluated: 12/07/2015
Review Status: no assertion criteria provided
Related Genes: AP1G1   ATXN1L   IST1   PHLPP2   PKD1L3   ZNF821  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371671,697,752 - 72,032,231CLINVAR
Cytogenetic Map1616q22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14351042
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-05
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.