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Variant : CV606933 (GRCh37/hg19 17q25.3(chr17:79828248-81057996)x1) Homo sapiens

Symbol: CV606933
Name: GRCh37/hg19 17q25.3(chr17:79828248-81057996)x1
Condition: not provided [RCV000752233]
Clinical Significance: pathogenic
Last Evaluated: 02/04/2015
Review Status: no assertion criteria provided
Related Genes: ALYREF   ANAPC11   ARHGDIA   ASPSCR1   B3GNTL1   CCDC57   CD7   CENPX   CSNK1D   CYBC1   DCXR   DUS1L   FASN   FN3K   FN3KRP   FOXK2   GPS1   HEXD   HEXD-IT1   LRRC45   MAFG   METRNL   MYADML2   NARF   NOTUM   NPB   OGFOD3   PCYT2   PYCR1   RAB40B   RAC3   RFNG   SECTM1   SIRT7   SLC16A3   TBCD   TEX19   UTS2R   WDR45B   ZNF750  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371779,828,248 - 81,057,996CLINVAR
Cytogenetic Map1717q25.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14367557
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-03-31
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.