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Variant : CV382236 (GRCh37/hg19 5q14.1(chr5:79678575-80868550)x3) Homo sapiens

Symbol: CV382236
Name: GRCh37/hg19 5q14.1(chr5:79678575-80868550)x3
Condition: See cases [RCV000448914]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: ACOT12   ANKRD34B   CKMT2   DHFR   FAM151B   MSH3   MTRNR2L2   RASGRF2   SSBP2   ZCCHC9   ZFYVE16  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37579,678,575 - 80,868,550CLINVAR
Cytogenetic Map55q14.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853614
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-06-23
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.