dtl[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
nsv3890097	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 108,938,253-108,951,786 , GRCh38.p12 chr13: 108,285,905-108,299,438	RNA5SP39, TNFSF13B
nsv3890910	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 108,938,253-108,951,595 , GRCh38.p12 chr13: 108,285,905-108,299,247	TNFSF13B, RNA5SP39
nsv3892878	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 108,947,088-108,951,999 , GRCh38.p12 chr13: 108,294,740-108,299,651	TNFSF13B, RNA5SP39
nsv3908671	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 108,926,989-108,951,786 , GRCh38.p12 chr13: 108,274,641-108,299,438	TNFSF13B, RNA5SP39
nsv3896767	copy number variation	1	nstd102	human	Benign	GRCh37 chr13: 108,926,989-108,951,595 , GRCh38.p12 chr13: 108,274,641-108,299,247	RNA5SP39, TNFSF13B
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	RNU6-71P, LINC00676, 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	LOC105370271, OR7E33P, 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	TEX30, LOC101927712, 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	GPC5, SNORD31B, 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	MIR4705, LOC102724149, 430 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	LOC107984609, SOX21, 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	ZIC2, LOC101060553, 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	TMTC4, COL4A2, 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	RPL15P18, FGF14-AS1, 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	RPS6P23, LOC105370344, 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	ZIC2, LINC03032, 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	LOC107984609, LINC00354, 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	LINC00359, LOC107984609, 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	DOCK9, RNU1-24P, 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	LOC107984615, ARGLU1, 189 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 131

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Number of Variants: 20

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