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Variant : CV437106 (GRCh37/hg19 16p13.3(chr16:3146027-6362229)x1) Homo sapiens

Symbol: CV437106
Name: GRCh37/hg19 16p13.3(chr16:3146027-6362229)x1
Condition: See cases [RCV000511703]
Clinical Significance: pathogenic
Last Evaluated: 09/12/2014
Review Status: no assertion criteria provided
Related Genes: ADCY9   ALG1   ANKS3   C16orf71   C16orf89   C16orf90   C16orf96   CDIP1   CLUAP1   CORO7   CORO7-PAM16   CREBBP   DNAJA3   DNASE1   EEF2KMT   GLIS2   GLYR1   HMOX2   MEFV   MGRN1   MTRNR2L4   NAA60   NAGPA   NLRC3   NMRAL1   NUDT16L1   OR1F1   OR2C1   PAM16   PPL   RBFOX1   ROGDI   SEC14L5   SEPTIN12   SLX4   SMIM22   SRL   TFAP4   TIGD7   TRAP1   UBALD1   UBN1   VASN   ZNF174   ZNF200   ZNF205   ZNF213   ZNF263   ZNF500   ZNF597   ZNF75A   ZSCAN32  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37163,146,027 - 6,362,229CLINVAR
Cytogenetic Map1616p13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13463032
Created: 2017-12-12
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.