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Variant : CV165311 (GRCh38/hg38 16q24.1-24.3(chr16:86950106-89335814)x1) Homo sapiens

Symbol: CV165311
Name: GRCh38/hg38 16q24.1-24.3(chr16:86950106-89335814)x1
Condition: See cases [RCV000143624]
Clinical Significance: pathogenic
Last Evaluated: 10/01/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACSF3   ANKRD11   APRT   BANP   C16orf95   CA5A   CBFA2T3   CDH15   CDT1   CTU2   CYBA   FBXO31   GALNS   IL17C   JPH3   KLHDC4   LINC00304   LINC02138   LINC02181   LINC02182   LOC100289580   LOC339059   MAP1LC3B   MIR11401   MIR4722   MIR5189   MIR6775   MVD   PABPN1L   PIEZO1   RNF166   SLC22A31   SLC7A5   SNAI3   SNAI3-AS1   TRAPPC2L   TRM-CAT6-1   ZC3H18   ZC3H18-AS1   ZCCHC14   ZFPM1   ZNF469   ZNF778  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_86950106)_(89335814_?)del
NC_000016.9:g.(?_86983712)_(89402222_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381686,950,106 - 89,335,814CLINVAR
GRCh371686,983,712 - 89,402,222CLINVAR
Build 361685,541,213 - 87,929,723CLINVAR
Cytogenetic Map1616q24.1-24.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491222
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.