dbVar for Gene (Select 91057) - 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
nsv5864180	copy number variation	1	nstd209	human		GRCh38 chr11: 27,356,026-27,359,062 , GRCh37.p13 chr11: 27,377,573-27,380,609	CCDC34
nsv5860980	copy number variation	1	nstd209	human		GRCh38 chr11: 27,340,461-27,351,571 , GRCh37.p13 chr11: 27,362,008-27,373,118	CCDC34
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv4984322	copy number variation	1	nstd200	human		GRCh38 chr11: 27,325,664-27,350,124 , GRCh37.p13 chr11: 27,347,211-27,371,671	CCDC34
nsv4978828	copy number variation	1	nstd200	human		GRCh38 chr11: 27,359,357-27,364,538 , GRCh37.p13 chr11: 27,380,904-27,386,085	CCDC34, LGR4
nsv4843064	copy number variation	1	nstd200	human		GRCh37 chr11: 27,347,211-27,371,671 , GRCh38.p12 chr11: 27,325,664-27,350,124	CCDC34
nsv4841453	copy number variation	1	nstd200	human		GRCh37 chr11: 27,360,909-27,370,392 , GRCh38.p12 chr11: 27,339,362-27,348,845	CCDC34
nsv4751865	inversion	1	nstd199	human		GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187	, ACP2, 1686 more genes
nsv4741272	copy number variation	1	nstd199	human		GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605	, DRAP1, 1535 more genes
nsv4675502	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 13,970,757-27,565,888 , GRCh38.p12 chr11: 13,949,210-27,544,341	MRGPRX5P, LDHC, 171 more genes
nsv4674879	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449	BGLT3, RPL21P97, 723 more genes
nsv4674824	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,053,978-34,732,891 , GRCh38.p12 chr11: 11,032,431-34,711,344	SNORA88, LINC02729, 305 more genes
nsv4614832	copy number variation	1	nstd183	human		GRCh37 chr11: 27,370,853-27,375,294 , GRCh38.p12 chr11: 27,349,306-27,353,747	CCDC34
nsv4601051	copy number variation	1	nstd183	human		GRCh37 chr11: 27,360,671-27,362,184 , GRCh38.p12 chr11: 27,339,124-27,340,637	CCDC34
nsv4482020	mobile element insertion	1	nstd166	human		GRCh37.p13 chr11: 27,379,396-27,379,396 , GRCh38.p12 chr11: 27,357,849-27,357,849	CCDC34
nsv4480596	mobile element insertion	1	nstd166	human		GRCh37.p13 chr11: 27,375,771-27,375,771 , GRCh38.p12 chr11: 27,354,224-27,354,224	CCDC34
nsv4455873	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097	DNAJC24, LOC102723568, 153 more genes
nsv4211589	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 27,372,893-27,373,496 , GRCh38.p12 chr11: 27,351,346-27,351,949	CCDC34
nsv4196395	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 27,360,909-27,370,392 , GRCh38.p12 chr11: 27,339,362-27,348,845	CCDC34
nsv3922794	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119	LOC107984419, LINC02758, 150 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

Links from Gene

Items: 1 to 20 of 131

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Number of Variants: 20

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