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Variant : CV614057 (GRCh37/hg19 15q26.2-26.3(chr15:96873212-102389423)) Homo sapiens

Symbol: CV614057
Name: GRCh37/hg19 15q26.2-26.3(chr15:96873212-102389423)
Condition: not provided [RCV000767761]
Clinical Significance: pathogenic
Last Evaluated: 11/01/2018
Review Status: criteria provided, single submitter
Related Genes: ADAMTS17   ALDH1A3   ARRDC4   ASB7   CERS3   CHSY1   FAM169B   IGF1R   LINS1   LRRC28   LRRK1   LYSMD4   MEF2A   NR2F2   OR4F15   OR4F6   PCSK6   PGPEP1L   SELENOS   SNRPA1   SPATA8   SYNM   TARSL2   TM2D3   TTC23  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371596,873,212 - 102,389,423CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14399713
Created: 2019-05-07
Species: Homo sapiens
Last Modified: 2019-08-06
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.