nsv1398044 - dbVar - NCBI

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Result Filters

Variant type:: copy number variation

Associated study:: nstd102

Organism:
human

Genes(s) in region:: LONRF2P5; RHOT1P2; LOC105372747; LOC105372750; ADAMTS1; MARCKSP1; RBM11; RNU4-45P; RPL39P40; LOC100420035; LINC00320; RPL13AP7; LOC654338; SNORD74B; RNU6-123P; LINC01689; BTG3; GXYLT1P2; LOC100419737; LOC105372753; TRG-GCC1-5; LOC107985482; MIR548X; TUBAP1; ADAMTS5; GRAMD4P1; MIR155HG; LOC105369292; RPL37P3; MIR548XHG; NEK4P1; RNU6-926P; ANKRD20A11P; PPP6R2P1; LOC112268283; LOC107985490; ATP5PF; GPX1P2; ZNF299P; NRIP1; LOC107985516; NIPA2P3; LINC01687; TMPRSS15; FRG2MP; VDAC2P1; CYP4F29P; EIF4A1P1; LINC00158; CHODL-AS1; RNU6-1326P; HSPA13; BTG3-AS1; C21orf91-OT1; CYYR1; CYCSP42; GTF2IP2; SREK1IP1P1; LINC01692; C1QBPP1; RN7SL163P; TERF1P1; RNA5SP489; RNU1-139P; GAPDHP16; NF1P3; CYP2C63P; MIR3156-3; VN1R8P; KRT18P2; LOC107985508; LOC107985511; LOC107985474; RBPMSLP; RNU6-954P; LOC105372745; LOC105372759; LOC105372756; FDX1P2; LINC01425; LOC107985494; MIR155; NCSTNP1; LOC105369304; GABPA; LOC102724355; SNX18P13; ANKRD20A18P; CNN2P7; LOC105372762; POLR2CP1; PPIAP1; RNU1-98P; LOC105372757; MAPK6P2; LINC01549; RN7SKP236; LIPI; ERLEC1P1; RNU6-772P; MIR125B2; LOC105369302; ANKRD30BP1; MSANTD2P1; MIR4759; CHODL; LOC110091776; USP25; RBMX2P1; LLPHP2; LINC00308; MIR6130; RPL10P1; LINC01684; RNU6-113P; CYYR1-AS1; LINC00317; LOC105377134; FAM207CP; JAM2; LOC107985483; MIR99A; C21orf91; OR4K11P; PPIAP22; LOC105372760; MIR99AHG; FEM1AP1; FGF7P2; SAMSN1-AS1; RPS3AP1; LINC01673; LOC105372740; VN2R20P; ASMER1; LOC107985512; RAD23BP3; RNA5SP488; LOC101927745; MIR3118-1; RNU6-286P; NCAM2; LOC105372738; MIR8069; RPS26P5; LOC105372749; LINC01683; OR4K12P; SNX19P1; CXADR; ABCC13; MIRLET7C; APP; RN7SKP147; EEF1A1P1; FDPSP6; LINC02573; LINC01674; POTED; ZNF114P1; LINC00515; SAMSN1; LINC00113; D21S2088E; MRPL39; RNU6-426P; CXADRP1; RPL37P4; LOC105372758; SLC6A6P1; BTF3L4P1; RNU2-55P; RNGTTP1; See more...

Location information:

Clinical significance:

ID:: 30347707

variant

Supplemental Content

Related information

ClinVar
Clinical reports for this variation
Functional Class
Functional class of the sequence domain architecture
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Link from dbVar to Gene
OMIM
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Pathways + GO
Pathways, annotations and biological systems (BioSystems) that cite genes containing current variations.
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J Obach (1)
dbVar
LOC481709 [Canis lupus familiaris]
LOC481709 [Canis lupus familiaris]
Gene ID:481709

Gene
Friesodielsia maclellandii (0)
Biocollections
Conserved Domain Links for Protein (Select 21704168) (2)
Conserved Domains
Potentilla nurensis (0)
ClinVar

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