bub1b[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
nsv7094369	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 40,453,422-40,457,417 , GRCh38.p12 chr15: 40,161,221-40,165,216	BUB1B
nsv6309787	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 40,457,244-40,457,407 , GRCh38.p12 chr15: 40,165,043-40,165,206	BUB1B
nsv4682798	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr15: 40,475,905-40,477,853 , GRCh38.p12 chr15: 40,183,704-40,185,652	BUB1B, LOC107984763
nsv4675567	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 40,499,508-40,566,902 , GRCh38.p12 chr15: 40,207,307-40,274,701	BUB1B, PAK6-AS1, 3 more genes
nsv3878886	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 40,453,416-40,512,966 , GRCh38 chr15: 40,161,215-40,220,765	BUB1B, LOC107984763, 1 more genes
nsv6309724	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 40,453,422-40,512,960 , GRCh38.p12 chr15: 40,161,221-40,220,759	BUB1B, BUB1B-PAK6, 1 more genes
nsv3916249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189	BUB1B, H3P40, 1616 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	BUB1B, RNU6-18P, 1442 more genes
nsv3915967	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 32,635,803-40,233,825 , GRCh37 chr15: 32,928,004-40,526,026 , NCBI36 chr15: 30,715,296-38,313,318	BUB1B, ANP32AP1, 112 more genes
nsv3903574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 38,170,429-40,775,075 , GRCh38.p12 chr15: 37,878,228-40,482,876	BUB1B, CHST14, 49 more genes
nsv3900281	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337	BUB1B, MYZAP, 1750 more genes
nsv3913581	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189	BUB1B, MIR4513, 1754 more genes
nsv3904086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959	BUB1B, TMEM202, 1747 more genes
nsv3905138	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413	BUB1B, FES, 1738 more genes
nsv3892955	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909	BUB1B, FAM81A, 1614 more genes
nsv3876912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654	BUB1B, RNU6-953P, 1385 more genes
nsv4436396	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr15: 34,346,036-41,764,885 , GRCh37 chr15: 34,638,237-42,057,083	BUB1B, ACTC1, 150 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	BUB1B, SNRPCP18, 1622 more genes
nsv3918644	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	BUB1B, SNORD116-23, 1622 more genes
nsv3911945	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,203,424-100,338,915 , GRCh37.p13 chr15: 22,652,060-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	BUB1B, HDDC3, 1622 more genes

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Number of Variants: 20

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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

Search results

Items: 1 to 20 of 27

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity