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Variant : CV247782 (GRCh37/hg19 3p25.3(chr3:9405337-10168892)x3) Homo sapiens

Symbol: CV247782
Name: GRCh37/hg19 3p25.3(chr3:9405337-10168892)x3
Condition: See cases [RCV000240180]
Clinical Significance: likely pathogenic
Last Evaluated: 01/20/2016
Review Status: criteria provided, single submitter
Related Genes: ARPC4   ARPC4-TTLL3   BRK1   BRPF1   CAMK1   CIDEC   CPNE9   CRELD1   EMC3   FANCD2   FANCD2OS   IL17RC   IL17RE   JAGN1   LHFPL4   MTMR14   OGG1   PRRT3   RPUSD3   SETD5   TADA3   THUMPD3   TTLL3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3739,405,337 - 10,168,892CLINVAR
Cytogenetic Map33p25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 11541675
Created: 2016-10-11
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.