dnz1[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
nsv3907801	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 14,686,308-14,688,410 , GRCh38.p12 chr9: 14,686,310-14,688,412	ZDHHC21
nsv3904846	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 14,686,950-14,688,410 , GRCh38.p12 chr9: 14,686,952-14,688,412	ZDHHC21
nsv3894415	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 14,590,805-14,677,538 , GRCh38.p12 chr9: 14,590,807-14,677,540	CDCA4P1, ZDHHC21
nsv3903924	copy number variation	1	nstd102	human	Benign	GRCh37 chr9: 14,686,308-14,790,363 , GRCh38.p12 chr9: 14,686,310-14,790,365	ZDHHC21, FREM1, 1 more genes
nsv4675012	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 14,670,160-14,871,548 , GRCh38.p12 chr9: 14,670,162-14,871,550	LOC105375979, FREM1, 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	RPL4P5, SMARCA2, 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	LOC107987049, RNU2-47P, 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	ACTG1P14, DMAC1, 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	DOCK8-AS1, RN7SL25P, 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	RNA5SP279, CDC37L1, 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	DMAC1, RNU7-185P, 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	LINC02851, LOC105375971, 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	RANBP6, CDCA4P1, 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	GLIS3, LDHAP4, 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	RPS26P3, CDC37L1-DT, 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	FTH1P12, RIC1, 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	ACTG1P14, CLCN3P1, 176 more genes
nsv3917732	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 214,367-16,307,944 , GRCh37 chr9: 214,367-16,307,942 , NCBI36 chr9: 204,367-16,297,942	RLN1, RNU6-246P, 173 more genes
nsv3919683	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 322,690-16,401,656 , NCBI36 chr9: 312,690-16,391,654 , GRCh37 chr9: 322,690-16,401,654	DMRT2, LINC01230, 172 more genes
nsv3918828	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,090-15,260,598 , NCBI36 chr9: 194,090-15,250,598 , GRCh38 chr9: 204,090-15,260,600	HMGN2P31, GLIS3-AS2, 160 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 113

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Number of Variants: 20

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