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Variant : CV436628 (GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1) Homo sapiens

Symbol: CV436628
Name: GRCh37/hg19 7q33-36.3(chr7:137917376-159119707)x1
Condition: See cases [RCV000511889]
Clinical Significance: pathogenic
Last Evaluated: 08/26/2015
Review Status: no assertion criteria provided
Related Genes: ABCB8   ABCF2   ACTR3B   ACTR3C   ADCK2   AGAP3   AGK   AOC1   ARHGEF35   ARHGEF5   ASB10   ASIC3   ATG9B   ATP6V0A4   ATP6V0E2   BRAF   C7orf33   CASP2   CDK5   CHPF2   CLCN1   CLEC2L   CLEC5A   CNPY1   CNTNAP2   CRYGN   CTAGE15   CTAGE4   CTAGE6   CTAGE8   CUL1   DENND11   DENND2A   DNAJB6   EN2   EPHA1   EPHB6   ESYT2   EZH2   FAM131B   FASTK   FMC1   FMC1-LUC7L2   GALNT11   GALNTL5   GBX1   GIMAP1   GIMAP2   GIMAP4   GIMAP5   GIMAP6   GIMAP7   GIMAP8   GSTK1   HTR5A   INSIG1   KCNH2   KDM7A   KEL   KIAA1549   KLRG2   KMT2C   KRBA1   LLCFC1   LMBR1   LRRC61   LUC7L2   MGAM   MIR671   MKRN1   MNX1   MRPS33   MTRNR2L6   NCAPG2   NDUFB2   NOBOX   NOM1   NOS3   NUB1   OR2A1   OR2A12   OR2A14   OR2A2   OR2A25   OR2A42   OR2A5   OR2A7   OR2F1   OR2F2   OR6B1   OR6V1   OR9A2   OR9A4   PARP12   PAXIP1   PDIA4   PIP   PRKAG2   PRSS1   PRSS37   PRSS58   PTPRN2   RAB19   RARRES2   RBM33   REPIN1   RHEB   RNF32   RNY1   RNY3   RNY4   RNY5   SHH   SLC37A3   SLC4A2   SMARCD3   SSBP1   SVOPL   TAS2R3   TAS2R38   TAS2R39   TAS2R4   TAS2R40   TAS2R41   TAS2R5   TAS2R60   TBXAS1   TCAF1   TCAF2   TMEM139   TMEM176A   TMEM176B   TMEM178B   TMEM213   TMUB1   TPK1   TRB   TRIM24   TRPV5   TRPV6   TTC26   UBE3C   UBN2   VIPR2   WDR60   WDR86   WEE2   XRCC2   ZBED6CL   ZC3HAV1   ZC3HAV1L   ZNF212   ZNF282   ZNF398   ZNF425   ZNF467   ZNF746   ZNF775   ZNF777   ZNF783   ZNF786   ZNF862   ZYX  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh377137,917,376 - 159,119,707CLINVAR
Cytogenetic Map77q33-36.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444858
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.