dbVar data for all organisms

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Variant Placements (including Supporting Variants) for nstd102 (displaying 100 of 172298 variants)
Study ID	Variant ID	Variant Region type	Variant Call type	Sampleset ID	Method	Analysis ID	Validation	Subject phenotype	Clinical Interpretation	Assembly	Accession	Chr	Outer-Start	Start	Inner-Start	Inner-End	End	Outer-End	Placement Type	Remap Score
nstd102	nssv15124731		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			14874	7467242		7467242	Remapped	1.00097
nstd102	nssv15126343		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1	762414		762414	2636399		2636399	Remapped	1.00211
nstd102	nssv15127013		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			14874	8785327		8785327	Remapped	1.00082
nstd102	nssv15127493		copy number loss	1	Multiple	Multiple	No	See cases	Benign	GRCh38.p12	NC_000001.11	1			585989	714397		743442	Remapped	0.61144
nstd102	nssv15128257		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1	778764		778764	2950871		2950871	Remapped	1.00874
nstd102	nssv15128480		copy number loss	1	Multiple	Multiple	No	See cases	Benign	GRCh38.p12	NC_000001.11	1	258946		258946	714338		714338	Remapped	1.08164
nstd102	nssv15129004		copy number gain	1	Multiple	Multiple	No	See cases	Uncertain significance	GRCh38.p12	NC_000001.11	1			14874	297968			Remapped	0.80018
nstd102	nssv15147705		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			811228	14750663			Remapped	0.97271
nstd102	nssv15149099		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	12639316			Remapped	0.99524
nstd102	nssv15150044		copy number gain	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			19225	4341631			Remapped	0.9863
nstd102	nssv15150122		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			629044	3665494			Remapped	1.00624
nstd102	nssv15156632		copy number loss	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	1101579			Remapped	1.06768
nstd102	nssv15156633		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			82154	1291132			Remapped	1.05647
nstd102	nssv15156634		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			82154	1354483			Remapped	1.05351
nstd102	nssv15156635		copy number loss	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	3424291			Remapped	1.0256
nstd102	nssv15156636		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			99236	297968			Remapped	0.63842
nstd102	nssv15156637		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			611476	650815			Remapped	1
nstd102	nssv15156638		copy number loss	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			778658	791018			Remapped	1
nstd102	nssv15156639		copy number loss	1	Multiple	Multiple	No	not provided	Uncertain significance	GRCh38.p12	NC_000001.11	1			789139	1229930			Remapped	1
nstd102	nssv15156678		copy number loss	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			47851	1229930			Remapped	1.05783
nstd102	nssv15156679		copy number loss	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			47851	6599812			Remapped	0.99092
nstd102	nssv15156680		copy number loss	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			80386	91719			Remapped	1
nstd102	nssv15156681		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			82154	912603			Remapped	1.08438
nstd102	nssv15156682		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			82154	1354455			Remapped	1.05351
nstd102	nssv15156683		copy number loss	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			624954	634798			Remapped	1
nstd102	nssv15156684		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			773384	903723			Remapped	1
nstd102	nssv15156967		copy number gain	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			47851	248934250			Remapped	0.99882
nstd102	nssv15156968		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			82154	932255			Remapped	1.08227
nstd102	nssv15156969		copy number loss	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	7876212			Remapped	0.99235
nstd102	nssv15156970		copy number gain	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	248924793			Remapped	0.99882
nstd102	nssv15169562		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			47851	778658			Remapped	1.097
nstd102	nssv15169563		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			790357	903723			Remapped	1
nstd102	nssv15169564		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			790357	1099368			Remapped	1
nstd102	nssv15169565		copy number loss	1	Multiple	Multiple	No	not provided	Likely benign	GRCh38.p12	NC_000001.11	1			791657	1431450			Remapped	1
nstd102	nssv15170259		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			817186	930314			Remapped	1
nstd102	nssv15171013		copy number loss	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			47851	91538			Remapped	1
nstd102	nssv15171014		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			791018	926428			Remapped	1
nstd102	nssv15171015		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			791101	818161			Remapped	1
nstd102	nssv15171016		copy number gain	1	Multiple	Multiple	No	not provided	Benign	GRCh38.p12	NC_000001.11	1			791101	945526			Remapped	1
nstd102	nssv15605943		copy number loss	1	Multiple	Multiple	No	1p36 deletion syndrome;CHROMOSOME 1p36 DELETION SYNDROME;Chromosome 1p36 Deletion Syndrome;Chromosome 1p36 deletion syndrome	Pathogenic	GRCh38.p12	NC_000001.11	1			633328	3746385			Remapped	1.00608
nstd102	nssv15605944		copy number loss	1	Multiple	Multiple	No	1p36 deletion syndrome;CHROMOSOME 1p36 DELETION SYNDROME;Chromosome 1p36 Deletion Syndrome;Chromosome 1p36 deletion syndrome	Pathogenic	GRCh38.p12	NC_000001.11	1			633328	2636393			Remapped	1.00197
nstd102	nssv15605988		copy number loss	1	Multiple	Multiple	No	not provided	Likely pathogenic	GRCh38.p12	NC_000001.11	1			633328	1348399			Remapped	1
nstd102	nssv15755176		deletion	1	Multiple	Multiple	No	Neurodevelopmental Disorders;Neurodevelopmental disorder	Pathogenic	GRCh38.p12	NC_000001.11	1		618995			9719784		Remapped	0.98649
nstd102	nssv15755708		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	7577000			Remapped	0.99205
nstd102	nssv15755716		copy number loss	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	11724061			Remapped	0.99487
nstd102	nssv15774998		copy number gain	1	Multiple	Multiple	No	not provided	Uncertain significance	GRCh38.p12	NC_000001.11	1			792351	2176419			Remapped	1.00286
nstd102	nssv16208658		copy number gain	1	Multiple	Multiple	No	See cases	Pathogenic	GRCh38.p12	NC_000001.11	1			82154	3432949			Remapped	1.02554
nstd102	nssv16255736		copy number loss	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			10001	5532775			Remapped	0.98747
nstd102	nssv18792863		copy number loss	1	Multiple	Multiple	No	1p36 deletion syndrome;CHROMOSOME 1p36 DELETION SYNDROME;Chromosome 1p36 Deletion Syndrome;Chromosome 1p36 deletion syndrome	Pathogenic	GRCh38.p12	NC_000001.11	1			10001			2649537	Remapped	1.02269
nstd102	nssv18830721		copy number loss	1	Multiple	Multiple	No	not provided	Pathogenic	GRCh38.p12	NC_000001.11	1			601397	5952836			Remapped	0.97723
nstd102	nsv3872448	copy number variation					No			GRCh38.p12	NC_000001.11	1			99236	297968			Remapped	0.63842
nstd102	nsv3872574	copy number variation					No			GRCh38.p12	NC_000001.11	1			778658	791018			Remapped	1
nstd102	nsv3872616	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	1354483			Remapped	1.05351
nstd102	nsv3872668	copy number variation					No			GRCh38.p12	NC_000001.11	1			789139	1229930			Remapped	1
nstd102	nsv3872984	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	1101579			Remapped	1.06768
nstd102	nsv3873030	copy number variation					No			GRCh38.p12	NC_000001.11	1			811228	14750663			Remapped	0.97271
nstd102	nsv3874222	copy number variation					No			GRCh38.p12	NC_000001.11	1			611476	650815			Remapped	1
nstd102	nsv3874379	copy number variation					No			GRCh38.p12	NC_000001.11	1			791101	945526			Remapped	1
nstd102	nsv3875326	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	1291132			Remapped	1.05647
nstd102	nsv3875881	copy number variation					No			GRCh38.p12	NC_000001.11	1			624954	634798			Remapped	1
nstd102	nsv3877120	copy number variation					No			GRCh38.p12	NC_000001.11	1			773384	903723			Remapped	1
nstd102	nsv3877224	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	912603			Remapped	1.08438
nstd102	nsv3877322	copy number variation					No			GRCh38.p12	NC_000001.11	1			47851	6599812			Remapped	0.99092
nstd102	nsv3877365	copy number variation					No			GRCh38.p12	NC_000001.11	1			47851	248934250			Remapped	0.99882
nstd102	nsv3877630	copy number variation					No			GRCh38.p12	NC_000001.11	1			791101	818161			Remapped	1
nstd102	nsv3878412	copy number variation					No			GRCh38.p12	NC_000001.11	1			80386	91719			Remapped	1
nstd102	nsv3878647	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	932255			Remapped	1.08227
nstd102	nsv3878985	copy number variation					No			GRCh38.p12	NC_000001.11	1			47851	1229930			Remapped	1.05783
nstd102	nsv3879191	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	1354455			Remapped	1.05351
nstd102	nsv3879888	copy number variation					No			GRCh38.p12	NC_000001.11	1			817186	930314			Remapped	1
nstd102	nsv3881642	copy number variation					No			GRCh38.p12	NC_000001.11	1			19225	4341631			Remapped	0.9863
nstd102	nsv3882000	copy number variation					No			GRCh38.p12	NC_000001.11	1			791657	1431450			Remapped	1
nstd102	nsv3882640	copy number variation					No			GRCh38.p12	NC_000001.11	1			629044	3665494			Remapped	1.00624
nstd102	nsv3882983	copy number variation					No			GRCh38.p12	NC_000001.11	1			790357	903723			Remapped	1
nstd102	nsv3883849	copy number variation					No			GRCh38.p12	NC_000001.11	1			791018	926428			Remapped	1
nstd102	nsv3885153	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	7876212			Remapped	0.99235
nstd102	nsv3885206	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	248924793			Remapped	0.99882
nstd102	nsv3886255	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	3424291			Remapped	1.0256
nstd102	nsv3887654	copy number variation					No			GRCh38.p12	NC_000001.11	1			47851	778658			Remapped	1.097
nstd102	nsv3888433	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	12639316			Remapped	0.99524
nstd102	nsv3889387	copy number variation					No			GRCh38.p12	NC_000001.11	1			47851	91538			Remapped	1
nstd102	nsv3889926	copy number variation					No			GRCh38.p12	NC_000001.11	1			790357	1099368			Remapped	1
nstd102	nsv3909879	copy number variation					No			GRCh38.p12	NC_000001.11	1			14874	297968			Remapped	0.80018
nstd102	nsv3913374	copy number variation					No			GRCh38.p12	NC_000001.11	1			14874	8785327		8785327	Remapped	1.00082
nstd102	nsv3917903	copy number variation					No			GRCh38.p12	NC_000001.11	1	258946		258946	714338		714338	Remapped	1.08164
nstd102	nsv3919515	copy number variation					No			GRCh38.p12	NC_000001.11	1			585989	714397		743442	Remapped	0.61144
nstd102	nsv3922337	copy number variation					No			GRCh38.p12	NC_000001.11	1	762414		762414	2636399		2636399	Remapped	1.00211
nstd102	nsv3922447	copy number variation					No			GRCh38.p12	NC_000001.11	1	778764		778764	2950871		2950871	Remapped	1.00874
nstd102	nsv3924689	copy number variation					No			GRCh38.p12	NC_000001.11	1			14874	7467242		7467242	Remapped	1.00097
nstd102	nsv4346794	copy number variation					No			GRCh38.p12	NC_000001.11	1			633328	2636393			Remapped	1.00197
nstd102	nsv4347035	copy number variation					No			GRCh38.p12	NC_000001.11	1			633328	1348399			Remapped	1
nstd102	nsv4347036	copy number variation					No			GRCh38.p12	NC_000001.11	1			633328	3746385			Remapped	1.00608
nstd102	nsv4435992	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	7577000			Remapped	0.99205
nstd102	nsv4436105	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	11724061			Remapped	0.99487
nstd102	nsv4436631	copy number variation					No			GRCh38.p12	NC_000001.11	1		618995			9719784		Remapped	0.98649
nstd102	nsv4452164	copy number variation					No			GRCh38.p12	NC_000001.11	1			792351	2176419			Remapped	1.00286
nstd102	nsv4674646	copy number variation					No			GRCh38.p12	NC_000001.11	1			82154	3432949			Remapped	1.02554
nstd102	nsv4728187	copy number variation					No			GRCh38.p12	NC_000001.11	1			10001	5532775			Remapped	0.98747
nstd102	nsv7099018	copy number variation					No			GRCh38.p12	NC_000001.11	1			10001			2649537	Remapped	1.02269
nstd102	nsv7137045	copy number variation					No			GRCh38.p12	NC_000001.11	1			601397	5952836			Remapped	0.97723

dbVar

Database of genomic structural variation

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