dbVar for Gene (Select 7365) - 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
nsv5898936	copy number variation	1	nstd209	human		GRCh38 chr4: 68,819,468-68,820,435 , GRCh37.p13 chr4: 69,685,186-69,686,153	UGT2B10
nsv5893654	copy number variation	1	nstd209	human		GRCh38 chr4: 68,803,443-68,843,217 , GRCh37.p13 chr4: 69,669,161-69,708,935	LOC100422189, UGT2B10
nsv5893576	copy number variation	1	nstd209	human		GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755	, DCK, 147 more genes
nsv5893478	copy number variation	1	nstd209	human		GRCh38 chr4: 68,744,526-68,822,038 , GRCh37.p13 chr4: 69,610,244-69,687,756	UGT2B10, LOC100422026, 1 more genes
nsv5840085	copy number variation	2	nstd209	human		GRCh38 chr4: 68,811,821-68,823,536 , GRCh37.p13 chr4: 69,677,539-69,689,254	LOC100422189, UGT2B10
nsv5840084	copy number variation	2	nstd209	human		GRCh38 chr4: 68,809,771-68,822,524 , GRCh37.p13 chr4: 69,675,489-69,688,242	UGT2B10, LOC100422189
nsv5840034	copy number variation	2	nstd209	human		GRCh38 chr4: 68,819,201-68,838,015 , GRCh37.p13 chr4: 69,684,919-69,703,733	UGT2B10
nsv5839463	copy number variation	2	nstd209	human		GRCh38 chr4: 68,810,621-68,816,485 , GRCh37.p13 chr4: 69,676,339-69,682,203	UGT2B10, LOC100422189
nsv5674237	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872	FTLP10, RNU6-410P, 335 more genes
nsv5668808	inversion	1	nstd207	human		GRCh38 chr4: 68,826,255-68,849,811 , GRCh37.p13 chr4: 69,691,973-69,715,529	UGT2B10
nsv5554461	sequence alteration	1	nstd206	human		GRCh38 chr4: 68,827,323-69,009,082 , GRCh37.p13 chr4: 69,693,041-69,874,800	UGT2B10, UGT2A3, 5 more genes
nsv5473841	copy number variation	1	nstd206	human		GRCh38 chr4: 68,803,448-68,843,218 , GRCh37.p13 chr4: 69,669,166-69,708,936	LOC100422189, UGT2B10
nsv5468832	copy number variation	1	nstd206	human		GRCh38 chr4: 68,813,000-68,852,000 , GRCh37.p13 chr4: 69,678,718-69,717,718	UGT2B10, LOC100422189
nsv5468413	copy number variation	1	nstd206	human		GRCh38 chr4: 68,819,469-68,820,436 , GRCh37.p13 chr4: 69,685,187-69,686,154	UGT2B10
nsv5461977	copy number variation	1	nstd206	human		GRCh38 chr4: 68,829,748-68,829,855 , GRCh37.p13 chr4: 69,695,466-69,695,573	UGT2B10
nsv5166201	mobile element insertion	1	nstd203	human		GRCh38 chr4: 68,817,627-68,817,641 , GRCh37.p13 chr4: 69,683,345-69,683,359	UGT2B10
nsv5034204	inversion	1	nstd200	human		GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231	, LOC100129728, 913 more genes
nsv4925754	copy number variation	1	nstd200	human		GRCh38 chr4: 68,795,160-69,345,433 , GRCh37.p13 chr4: 69,660,878-70,211,151	UGT2B28, SPOPLP3, 21 more genes
nsv4922809	copy number variation	1	nstd200	human		GRCh38 chr4: 68,819,469-68,820,436 , GRCh37.p13 chr4: 69,685,187-69,686,154	UGT2B10
nsv4922808	copy number variation	1	nstd200	human		GRCh38 chr4: 68,813,098-68,814,875 , GRCh37.p13 chr4: 69,678,816-69,680,593	LOC100422189, UGT2B10

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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

Links from Gene

Items: 1 to 20 of 292

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Number of Variants: 20

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