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Variant : CV675711 (GRCh37/hg19 16p13.3(chr16:4382314-4511029)x1) Homo sapiens

Symbol: CV675711
Name: GRCh37/hg19 16p13.3(chr16:4382314-4511029)x1
Condition: not provided [RCV000848810]
Clinical Significance: uncertain significance
Last Evaluated: 10/20/2017
Review Status: no assertion criteria provided
Related Genes: CORO7   CORO7-PAM16   DNAJA3   GLIS2   PAM16   VASN  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37164,382,314 - 4,511,029CLINVAR
Cytogenetic Map1616p13.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14980346
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-01-07
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.