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Variant : CV248444 (GRCh37/hg19 17q25.1(chr17:73870412-74160099)x3) Homo sapiens

Symbol: CV248444
Name: GRCh37/hg19 17q25.1(chr17:73870412-74160099)x3
Condition: See cases [RCV000240272]
Clinical Significance: uncertain significance
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ACOX1   CDK3   EVPL   EXOC7   FBF1   FOXJ1   GALR2   MRPL38   RNF157   SRP68   TEN1   TRIM47   TRIM65   ZACN  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371773,870,412 - 74,160,099CLINVAR
Cytogenetic Map1717q25.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541699
Created: 2016-10-11
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.