smarca2[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
nsv3897622	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 2,143,543-2,151,371 , GRCh38.p12 chr9: 2,143,543-2,151,371	SMARCA2
nsv3900012	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 2,149,063-2,151,371 , GRCh38.p12 chr9: 2,149,063-2,151,371	SMARCA2
nsv7097716	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,170,399-2,170,492 , GRCh38.p12 chr9: 2,170,399-2,170,492	SMARCA2
nsv7093292	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,047,296-2,047,379 , GRCh38 chr9: 2,047,296-2,047,379	SMARCA2
nsv7098448	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,181,551-2,192,739 , GRCh38.p12 chr9: 2,181,551-2,192,739	SMARCA2, LOC107987043
nsv4436408	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,074,076-2,381,053 , GRCh38.p12 chr9: 2,074,076-2,381,053	SMARCA2, LOC105375955, 3 more genes
nsv3893406	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 2,130,392-2,185,324 , GRCh38.p12 chr9: 2,130,392-2,185,324	SMARCA2, LOC107987043, 1 more genes
nsv6637244	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 1,627,292-2,217,469 , GRCh38.p12 chr9: 1,627,292-2,217,469	SMARCA2, LOC107987043, 3 more genes
nsv3920950	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,104-18,872,279 , GRCh37 chr9: 204,104-18,882,279 , GRCh38 chr9: 204,104-18,882,281	SMARCA2, RPL4P5, 193 more genes
nsv3910019	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 220,253-18,708,805 , NCBI36 chr9: 210,253-18,698,803 , GRCh37 chr9: 220,253-18,708,803	SMARCA2, LOC107987049, 191 more genes
nsv5381767	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-18,654,812 , GRCh38.p12 chr9: 204,193-18,654,814	SMARCA2, ACTG1P14, 191 more genes
nsv4768366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-18,073,357 , GRCh38.p12 chr9: 204,193-18,073,359	SMARCA2, DOCK8-AS1, 186 more genes
nsv3910119	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-18,063,357 , GRCh38 chr9: 204,193-18,073,359 , GRCh37 chr9: 204,193-18,073,357	SMARCA2, RNA5SP279, 186 more genes
nsv3917303	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 220,253-18,073,359 , GRCh37 chr9: 220,253-18,073,357 , NCBI36 chr9: 210,253-18,063,357	SMARCA2, DMAC1, 185 more genes
nsv4674929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-17,789,410 , GRCh38.p12 chr9: 203,861-17,789,412	SMARCA2, LINC02851, 184 more genes
nsv3905168	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-17,655,298 , GRCh38.p12 chr9: 203,861-17,655,300	SMARCA2, RANBP6, 184 more genes
nsv3899178	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 213,161-17,496,750 , GRCh38.p12 chr9: 213,161-17,496,752	SMARCA2, GLIS3, 181 more genes
nsv3903505	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-17,125,893 , GRCh38.p12 chr9: 203,861-17,125,895	SMARCA2, RPS26P3, 179 more genes
nsv3923785	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-16,887,578 , GRCh37 chr9: 204,193-16,897,578 , GRCh38 chr9: 204,193-16,897,580	SMARCA2, FTH1P12, 176 more genes
nsv3890932	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 203,861-16,856,907 , GRCh38.p12 chr9: 203,861-16,856,909	SMARCA2, ACTG1P14, 176 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 181

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Number of Variants: 20

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