upf3a[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
nsv3920069	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr13: 114,056,191-114,082,191 , GRCh37 chr13: 115,038,089-115,064,089 , GRCh38 chr13: 114,272,614-114,298,614	UPF3A, LOC105370384, 2 more genes
nsv3912307	copy number variation	1	nstd102	human	Benign	NCBI36 chr13: 114,016,663-114,072,815 , GRCh37 chr13: 114,998,561-115,054,713 , GRCh38 chr13: 114,233,086-114,289,238	UPF3A, CDC16, 3 more genes
nsv3915166	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr13: 114,245,917-114,293,574 , NCBI36 chr13: 114,029,494-114,077,151 , GRCh37 chr13: 115,011,392-115,059,049	UPF3A, CDC16, 2 more genes
nsv3910130	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr13: 114,242,325-114,282,241 , GRCh37 chr13: 115,007,800-115,047,716 , NCBI36 chr13: 114,025,902-114,065,818	UPF3A, LOC105370384, 3 more genes
nsv6291450	copy number variation	1	nstd102	human	not provided	GRCh37 chr13: 115,054,475-115,107,733 , GRCh38.p12 chr13: 114,289,000-114,342,258	UPF3A, LINC01054, 3 more genes
nsv3898583	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 115,054,633-115,107,733 , GRCh38.p12 chr13: 114,289,158-114,342,258	UPF3A, LOC112268113, 3 more genes
nsv3909860	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 115,064,062-115,085,141 , GRCh38 chr13: 114,298,587-114,327,173 , NCBI36 chr13: 114,082,164-114,110,750	UPF3A, CHAMP1, 1 more genes
nsv3919823	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr13: 114,022,754-114,069,808 , GRCh37.p13 chr13: 115,004,652-115,051,706 , GRCh38.p12 chr13: 114,239,177-114,286,231	UPF3A, LOC105370384, 3 more genes
nsv4768362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 114,893,728-115,093,115 , GRCh38.p12 chr13: 114,147,230-114,327,640	UPF3A, CDC16, 6 more genes
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	UPF3A, 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	UPF3A, 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	UPF3A, TEX30, 680 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	UPF3A, MIR4705, 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	UPF3A, 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	UPF3A, 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	UPF3A, 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	UPF3A, 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	UPF3A, 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	UPF3A, 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	UPF3A, LOC107984609, 265 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 130

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Number of Variants: 20

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