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Variant : CV672495 (GRCh37/hg19 5q14.1(chr5:79664621-80767791)x3) Homo sapiens

Symbol: CV672495
Name: GRCh37/hg19 5q14.1(chr5:79664621-80767791)x3
Condition: not provided [RCV000845611]
Clinical Significance: uncertain significance
Last Evaluated: 07/21/2017
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
GRCh37579,664,621 - 80,767,791CLINVAR
Cytogenetic Map55q14.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14976067
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-06-30
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.