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Variant : CV435367 (GRCh37/hg19 3p26.3-22.3(chr3:61891-33958201)x3) Homo sapiens

Symbol: CV435367
Name: GRCh37/hg19 3p26.3-22.3(chr3:61891-33958201)x3
Condition: See cases [RCV000510429]
Clinical Significance: pathogenic
Last Evaluated: 02/24/2015
Review Status: no assertion criteria provided
Related Genes: ANKRD28   ARL8B   ARPC4   ARPC4-TTLL3   ATG7   ATP2B2   AZI2   BHLHE40   BRK1   BRPF1   BTD   C3orf20   CAMK1   CAND2   CAPN7   CAV3   CCDC174   CCR4   CHCHD4   CHL1   CIDEC   CLASP2   CMC1   CMTM6   CMTM7   CMTM8   CNOT10   CNTN4   CNTN6   COLQ   CPNE9   CRBN   CRELD1   CRTAP   DAZL   DPH3   DYNC1LI1   EAF1   EDEM1   EFHB   EGOT   EMC3   EOMES   FANCD2   FANCD2OS   FBLN2   FBXL2   FGD5   FGD5-AS1   GADL1   GALNT15   GHRL   GHRLOS   GLB1   GPD1L   GRIP2   GRM7   HACL1   HDAC11   HRH1   IL17RC   IL17RE   IL5RA   IQSEC1   IRAK2   ITPR1   JAGN1   KAT2B   KCNH8   LHFPL4   LINC00312   LMCD1   LRRC3B   LRRN1   LSM3   METTL6   MKRN2   MRPS25   MTMR14   NEK10   NGLY1   NKIRAS1   NR1D2   NR2C2   NUP210   OGG1   OSBPL10   OXNAD1   OXSM   OXTR   PDCD6IP   PLCL2   PP2D1   PPARG   PRRT3   RAB5A   RAD18   RAF1   RARB   RBMS3   RBSN   RFTN1   RPL15   RPL32   RPUSD3   SATB1   SEC13   SETD5   SETMAR   SGO1   SH3BP5   SLC4A7   SLC6A1   SLC6A11   SLC6A6   SRGAP3   SSUH2   STT3B   SUMF1   SUSD5   SYN2   TADA3   TAMM41   TATDN2   TBC1D5   TGFBR2   THRB   THUMPD3   TIMP4   TMEM40   TMEM43   TMPPE   TOP2B   TRIM71   TRNT1   TSEN2   TTLL3   UBE2E1   UBE2E2   UBP1   VGLL4   VHL   WNT7A   XPC   ZCWPW2   ZNF385D   ZNF860  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37361,891 - 33,958,201CLINVAR
Cytogenetic Map33p26.3-22.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443408
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-20
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.