tuba8[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912287	copy number variation	1	nstd102	human	Benign	NCBI36 chr22: 16,989,960-17,031,614 , GRCh37 chr22: 18,609,960-18,651,614 , GRCh38 chr22: 18,127,193-18,168,847	TUBA8, USP18
nsv6311174	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,561,143-18,613,903 , GRCh38.p12 chr22: 18,078,377-18,131,136	TUBA8, PEX26, 1 more genes
nsv4674327	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,475,385-23,764,120 , GRCh38.p12 chr22: 17,992,619-23,421,933	TUBA8, GP1BB, 308 more genes
nsv4676119	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-20,730,144 , GRCh38.p12 chr22: 16,408,173-20,375,854	TUBA8, C22orf39, 150 more genes
nsv3923978	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,399,015-19,048,227 , GRCh37 chr22: 17,019,015-20,718,227 , GRCh38 chr22: 16,538,125-20,363,937	TUBA8, MIR185, 146 more genes
nsv4676296	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-20,125,005 , GRCh38.p12 chr22: 16,408,173-20,137,482	TUBA8, FAM230J, 139 more genes
nsv3895935	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-20,026,751 , GRCh38.p12 chr22: 16,408,174-20,039,228	TUBA8, FAM247C, 131 more genes
nsv3913197	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 17,397,498-20,708,934 , GRCh38 chr22: 16,916,608-20,354,644 , NCBI36 chr22: 15,777,498-19,038,934	TUBA8, E2F6P1, 128 more genes
nsv3910919	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-18,691,763 , GRCh37 chr22: 17,397,498-20,311,763 , GRCh38 chr22: 16,916,608-20,324,240	TUBA8, C22orf39, 127 more genes
nsv3923846	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,557,911-18,272,632 , GRCh37.p13 chr22: 17,177,911-19,892,632 , GRCh38.p12 chr22: 16,697,021-19,905,109	TUBA8, MIR648, 113 more genes
nsv7095928	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 17,565,982-20,052,185 , GRCh38.p12 chr22: 17,085,092-20,064,662	TUBA8, CA15P1, 103 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	TUBA8, LOC100419811, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	TUBA8, IGKV3OR22-2, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	TUBA8, RNU6-495P, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	TUBA8, FBXO7, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	TUBA8, FABP5P11, 1084 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	TUBA8, DDTL, 1084 more genes
nsv3890401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300	TUBA8, YPEL1, 1083 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	TUBA8, IGLV3-27, 1082 more genes
nsv3891895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410	TUBA8, POM121L7P, 1082 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

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Items: 1 to 20 of 78

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Number of Variants: 20

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