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Variant : CV436675 (GRCh37/hg19 17q25.1-25.2(chr17:73992637-75099218)x4) Homo sapiens

Symbol: CV436675
Name: GRCh37/hg19 17q25.1-25.2(chr17:73992637-75099218)x4
Condition: See cases [RCV000510197]
Clinical Significance: uncertain significance
Last Evaluated: 02/24/2015
Review Status: no assertion criteria provided
Related Genes: AANAT   CDK3   CYGB   EVPL   EXOC7   FOXJ1   GALR2   JMJD6   METTL23   MFSD11   MGAT5B   MXRA7   PRCD   PRPSAP1   QRICH2   RHBDF2   RNF157   SEC14L1   SPHK1   SRP68   SRSF2   ST6GALNAC1   ST6GALNAC2   TEN1   UBALD2   UBE2O   ZACN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371773,992,637 - 75,099,218CLINVAR
Cytogenetic Map1717q25.1-25.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443177
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-17
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.