fhl5[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
nsv6310652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 7,709,480-7,712,696 , GRCh38.p12 chr19: 7,644,594-7,647,810	STXBP2
nsv6310559	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 7,706,571-7,712,696 , GRCh38.p12 chr19: 7,641,685-7,647,810	STXBP2
nsv7095728	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr19: 7,703,306-7,707,110 , GRCh38.p12 chr19: 7,638,420-7,642,224	STXBP2
nsv6289793	copy number variation	1	nstd102	human	not provided	GRCh38 chr6: 144,176,889-144,196,079 , GRCh37.p13 chr6: 144,498,026-144,517,216	STX11
nsv3875313	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 7,637,130-7,647,830 , GRCh37 chr19: 7,702,016-7,712,716	STXBP2, PCP2
nsv4674830	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 97,061,871-97,115,085 , GRCh38.p12 chr6: 96,613,995-96,667,209	FHL5, TYMSP1, 2 more genes
nsv6310557	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 7,694,720-7,712,696 , GRCh38.p12 chr19: 7,629,834-7,647,810	PET100, PCP2, 2 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	FHL5, LOC107986534, 426 more genes
nsv6313858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488	FHL5, RN7SL509P, 311 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	FHL5, TUBE1, 318 more genes
nsv3876958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766	FHL5, LIN28B-AS1, 258 more genes
nsv3877239	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 94,202,605-109,878,834 , GRCh38.p12 chr6: 93,492,887-109,557,631	FHL5, RNA5SP211, 155 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	FHL5, RNU4-72P, 157 more genes
nsv3879439	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,576,950-104,658,245 , GRCh38.p12 chr6: 91,867,232-104,210,370	FHL5, FBXL4, 75 more genes
nsv6636338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 96,946,110-106,497,526 , GRCh38.p12 chr6: 96,498,234-106,049,651	FHL5, BVES-AS1, 74 more genes
nsv6636533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 96,596,732-105,554,568 , GRCh38.p12 chr6: 96,148,856-105,106,693	FHL5, MCHR2-AS1, 65 more genes
nsv7095726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 6,361,586-8,212,364 , GRCh38.p12 chr19: 6,361,575-8,147,480	SLC25A23, LYPLA2P2, 77 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	FHL5, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	FHL5, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	FHL5, SOD1P1, 2905 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

Search results

Items: 1 to 20 of 40

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Number of Variants: 20

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Supplemental Content

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