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Variant : CV436088 (GRCh37/hg19 15q26.2-26.3(chr15:98220018-102429112)x1) Homo sapiens

Symbol: CV436088
Name: GRCh37/hg19 15q26.2-26.3(chr15:98220018-102429112)x1
Condition: See cases [RCV000512353]
Clinical Significance: pathogenic
Last Evaluated: 10/22/2014
Review Status: no assertion criteria provided
Related Genes: ADAMTS17   ALDH1A3   ARRDC4   ASB7   CERS3   CHSY1   FAM169B   IGF1R   LINS1   LRRC28   LRRK1   LYSMD4   MEF2A   OR4F15   OR4F6   PCSK6   PGPEP1L   SELENOS   SNRPA1   SYNM   TARSL2   TM2D3   TTC23  
Variant Type: copy number loss (SO:0001743)
Evidence: clinical testing
HGVS Name(s): NC_000015.9:g.(?_98220018)_(102429112_?)del
Human AssemblyChrPosition (strand)Source
GRCh371598,220,018 - 102,429,112CLINVAR
Cytogenetic Map1515q26.2-26.3CLINVAR

References - uncurated

Additional Information

External Database Links
RGD Object Information
RGD ID: 13445317
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2019-08-06
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.