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Variant : CV625948 (GRCh37/hg19 15q13.2-13.3(chr15:30611102-32514341)x1) Homo sapiens

Symbol: CV625948
Name: GRCh37/hg19 15q13.2-13.3(chr15:30611102-32514341)x1
Condition: See cases [RCV000790595]
Clinical Significance: pathogenic
Last Evaluated: 10/26/2018
Review Status: criteria provided, single submitter
Related Genes: ARHGAP11B   CHRFAM7A   CHRNA7   FAN1   GOLGA8H   KLF13   MIR211   MTMR10   OTUD7A   TRPM1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371530,611,102 - 32,514,341CLINVAR
Cytogenetic Map1515q13.2-13.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14697851
Created: 2019-08-06
Species: Homo sapiens
Last Modified: 2019-10-08
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.