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Variant : CV159287 (GRCh38/hg38 3p25.3(chr3:8941623-10151752)x3) Homo sapiens

Symbol: CV159287
Name: GRCh38/hg38 3p25.3(chr3:8941623-10151752)x3
Condition: See cases [RCV000138535]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 08/13/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARPC4   ARPC4-TTLL3   BRK1   BRPF1   CAMK1   CIDEC   CPNE9   CRELD1   EMC3   EMC3-AS1   FANCD2   FANCD2OS   IL17RC   IL17RE   JAGN1   LHFPL4   MTMR14   OGG1   PRRT3   PRRT3-AS1   RAD18   RPUSD3   SETD5   SRGAP3   SRGAP3-AS2   SRGAP3-AS3   SRGAP3-AS4   TADA3   THUMPD3   THUMPD3-AS1   TTLL3   VHL  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_8941623)_(10151752_?)dup
NC_000003.11:g.(?_8983307)_(10193436_?)dup
NC_000003.10:g.(?_8958307)_(10168436_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3838,941,623 - 10,151,752CLINVAR
GRCh3738,983,307 - 10,193,436CLINVAR
Build 3638,958,307 - 10,168,436CLINVAR
Cytogenetic Map33p25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486075
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-04
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.