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Variant : CV676174 (GRCh37/hg19 7p22.3-22.2(chr7:36616-4298168)x1) Homo sapiens

Symbol: CV676174
Name: GRCh37/hg19 7p22.3-22.2(chr7:36616-4298168)x1
Condition: not provided [RCV000849273]
Clinical Significance: pathogenic
Last Evaluated: 06/19/2017
Review Status: no assertion criteria provided
Related Genes: ADAP1   AMZ1   BRAT1   C7orf50   CARD11   CHST12   COX19   CYP2W1   DNAAF5   EIF3B   ELFN1   FAM20C   GET4   GNA12   GPER1   GPR146   INTS1   IQCE   LFNG   MAD1L1   MAFK   MICALL2   MRM2   NUDT1   PDGFA   PRKAR1B   PSMG3   SDK1   SNX8   SUN1   TMEM184A   TTYH3   UNCX   ZFAND2A  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37736,616 - 4,298,168CLINVAR
Cytogenetic Map77p22.3-22.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14980791
Created: 2019-10-08
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.