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Variant : CV437170 (GRCh37/hg19 3p25.3(chr3:9600759-10000398)x3) Homo sapiens

Symbol: CV437170
Name: GRCh37/hg19 3p25.3(chr3:9600759-10000398)x3
Condition: See cases [RCV000512318]
Clinical Significance: likely benign
Last Evaluated: 07/15/2015
Review Status: no assertion criteria provided
Related Genes: ARPC4   ARPC4-TTLL3   BRPF1   CAMK1   CIDEC   CPNE9   CRELD1   IL17RC   IL17RE   JAGN1   MTMR14   OGG1   PRRT3   RPUSD3   TADA3   TTLL3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3739,600,759 - 10,000,398CLINVAR
Cytogenetic Map33p25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13445283
Created: 2017-11-07
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.