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Variant : CV72106 (GRCh37/hg19 14q32.3(chr14:106252705-106538480)x1) Homo sapiens

Symbol: CV72106
Name: GRCh37/hg19 14q32.3(chr14:106252705-106538480)x1
Condition: See cases [RCV000051222]
Clinical Significance: benign
Last Evaluated: 08/12/2011
Review Status: classified by single submitter|criteria provided, single submitter|no assertion criteria provided
Related Genes: FAM30A   IGH   IGHA1   IGHD   IGHD1-1   IGHD1-14   IGHD1-20   IGHD1-26   IGHD1-7   IGHD2-15   IGHD2-2   IGHD2-21   IGHD2-8   IGHD3-10   IGHD3-16   IGHD3-22   IGHD3-3   IGHD3-9   IGHD4-11   IGHD4-17   IGHD4-23   IGHD4-4   IGHD5-12   IGHD5-18   IGHD5-24   IGHD5-5   IGHD6-13   IGHD6-19   IGHD6-25   IGHD6-6   IGHD7-27   IGHG1   IGHG2   IGHG3   IGHG4   IGHJ1   IGHJ2   IGHJ3   IGHJ4   IGHJ5   IGHJ6   IGHM   IGHV1-2   IGHV1-3   IGHV6-1   MIR4507   MIR4537   MIR4538   MIR4539   MIR8071-1   MIR8071-2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NT_187600.1:g.(?_74094)_(475851_?)del
NC_000014.8:g.(?_106252705)_(106538480_?)del
NC_000014.7:g.(?_105143707)_(105609525_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3714106,252,705 - 106,538,480CLINVAR
Build 3614105,143,707 - 105,609,525CLINVAR
Cytogenetic Map1414q32.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 8618261
Created: 2014-05-13
Species: Homo sapiens
Last Modified: 2020-05-26
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.