arglu1[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
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	ARGLU1, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	ARGLU1, LOC105370271, 925 more genes
nsv4675850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,262,013-115,107,733 , GRCh38.p12 chr13: 52,687,878-114,342,258	ARGLU1, TEX30, 680 more genes
nsv3907697	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 53,551,300-109,850,651 , GRCh38.p12 chr13: 52,977,165-109,198,303	ARGLU1, GPC5, 565 more genes
nsv6314171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 79,370,012-115,107,733 , GRCh38.p12 chr13: 78,795,877-114,342,258	ARGLU1, MIR4705, 430 more genes
nsv3901091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 80,572,498-108,719,528 , GRCh38.p12 chr13: 79,998,363-108,067,180	ARGLU1, KRT18P27, 295 more genes
nsv3920102	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 86,788,927-114,340,331 , GRCh37 chr13: 87,441,182-115,085,141 , NCBI36 chr13: 86,239,183-114,123,908	ARGLU1, LOC107984609, 369 more genes
nsv3903376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 88,073,140-115,107,733 , GRCh38.p12 chr13: 87,420,885-114,342,258	ARGLU1, ZIC2, 364 more genes
nsv3896487	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 89,796,110-115,083,342 , GRCh38.p12 chr13: 89,143,856-114,317,867	ARGLU1, TMTC4, 347 more genes
nsv3890560	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,474,530-115,107,733 , GRCh38.p12 chr13: 93,822,277-114,342,258	ARGLU1, RPL15P18, 303 more genes
nsv3892450	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 96,586,481-115,107,733 , GRCh38.p12 chr13: 95,934,227-114,342,258	ARGLU1, RPS6P23, 268 more genes
nsv4675644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 96,895,656-115,107,733 , GRCh38.p12 chr13: 96,243,402-114,342,258	ARGLU1, ZIC2, 266 more genes
nsv6637400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258	ARGLU1, LOC107984609, 265 more genes
nsv5672796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,679,977-111,536,145 , GRCh38.p12 chr13: 94,027,723-110,883,798	ARGLU1, LINC00359, 220 more genes
nsv3914527	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 93,345,058-109,458,154 , NCBI36 chr13: 92,795,312-108,908,502 , GRCh37 chr13: 93,997,311-110,110,501	ARGLU1, DOCK9, 196 more genes
nsv3904662	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 94,703,767-109,731,879 , GRCh38.p12 chr13: 94,051,513-109,079,531	ARGLU1, LOC107984615, 189 more genes
nsv6314066	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 100,258,328-115,107,733 , GRCh38.p12 chr13: 99,606,074-114,342,258	ARGLU1, MIR4502, 208 more genes
nsv3905010	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 101,075,864-115,105,020 , GRCh38.p12 chr13: 100,423,610-114,339,545	ARGLU1, RN7SKP10, 194 more genes
nsv4728419	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 102,175,801-115,169,858 , GRCh38.p12 chr13: 101,523,450-114,344,403	ARGLU1, RPL7P45, 182 more genes
nsv3916756	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 100,987,397-114,110,750 , GRCh38 chr13: 101,537,045-114,327,173 , GRCh37 chr13: 102,189,396-115,085,141	ARGLU1, PROZ, 180 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 100

Page of 5

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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