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Variant : CV153910 (GRCh38/hg38 3p25.3(chr3:9624696-10039318)x1) Homo sapiens

Symbol: CV153910
Name: GRCh38/hg38 3p25.3(chr3:9624696-10039318)x1
Condition: See cases [RCV000133641]
Clinical Significance: uncertain significance
Last Evaluated: 09/18/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ARPC4   ARPC4-TTLL3   BRPF1   CAMK1   CIDEC   CPNE9   CRELD1   EMC3   EMC3-AS1   FANCD2   IL17RC   IL17RE   JAGN1   MTMR14   OGG1   PRRT3   PRRT3-AS1   RPUSD3   TADA3   TTLL3  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000003.12:g.(?_9624696)_(10039318_?)del
NC_000003.11:g.(?_9666380)_(10081002_?)del
NC_000003.10:g.(?_9641380)_(10056002_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh3839,624,696 - 10,039,318CLINVAR
GRCh3739,666,380 - 10,081,002CLINVAR
Build 3639,641,380 - 10,056,002CLINVAR
Cytogenetic Map33p25.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481226
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-19
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.