cldn10[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	CLDN10, 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	CLDN10, 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	CLDN10, 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	CLDN10, 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	CLDN10, 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	CLDN10, 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	CLDN10, 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	CLDN10, 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	CLDN10, TMTC4, 347 more genes
nsv3904416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 81,851,091-102,864,674 , GRCh38.p12 chr13: 81,276,956-102,212,324	CLDN10, TRF-GAA1-5, 224 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	CLDN10, RPL15P18, 303 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	CLDN10, 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	CLDN10, 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	CLDN10, LOC107984615, 189 more genes
nsv6637615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 93,535,335-105,788,229 , GRCh38.p12 chr13: 92,883,082-105,135,878	CLDN10, SNORD13G, 162 more genes
nsv3912597	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr13: 87,394,735-99,316,797 , GRCh38 chr13: 87,944,479-99,866,542 , GRCh37 chr13: 88,596,734-100,518,796	CLDN10, UGGT2, 151 more genes
nsv5672807	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 92,002,837-103,343,314 , GRCh38.p12 chr13: 91,350,583-102,690,964	CLDN10, RPL7L1P12, 153 more genes
nsv3918483	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 88,975,264-99,540,898 , NCBI36 chr13: 87,773,265-98,338,899 , GRCh38 chr13: 88,323,009-98,888,644	CLDN10, MTND6P18, 122 more genes
nsv3910040	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 89,549,510-96,657,834 , GRCh37 chr13: 90,201,764-97,310,088 , NCBI36 chr13: 88,999,765-96,108,089	CLDN10, LOC105370315, 77 more genes
nsv3918101	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 93,571,649-97,428,965 , NCBI36 chr13: 93,021,903-96,879,220 , GRCh37 chr13: 94,223,902-98,081,219	CLDN10, RNA5SP36, 48 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 82

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Number of Variants: 20

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Supplemental Content

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Search details

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