aga[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
nsv7096989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 178,351,918-178,357,515 , GRCh38.p12 chr4: 177,430,764-177,436,361	AGA
nsv7097243	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 178,357,420-178,363,667 , GRCh38.p12 chr4: 177,436,266-177,442,513	AGA, AGA-DT
nsv5673742	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 178,363,393-178,363,667 , GRCh38.p12 chr4: 177,442,239-177,442,513	AGA, AGA-DT
nsv3880905	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 178,376,638-178,385,199 , GRCh38.p12 chr4: 177,455,484-177,464,045	AGA-DT, RNA5SP172
nsv4683594	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 178,352,842-178,363,549 , GRCh38.p12 chr4: 177,431,688-177,442,395	AGA, AGA-DT
nsv6312246	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 178,352,862-178,363,529 , GRCh38.p12 chr4: 177,431,708-177,442,375	AGA, AGA-DT
nsv3914634	copy number variation	1	nstd102	human	Benign	NCBI36 chr4: 178,504,215-178,738,042 , GRCh37 chr4: 178,267,221-178,501,048 , GRCh38 chr4: 177,346,067-177,579,894	AGA, NEIL3, 3 more genes
nsv4729152	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 178,252,194-178,474,897 , GRCh38.p12 chr4: 177,331,040-177,553,743	AGA, AGA-DT, 3 more genes
nsv6634351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318	AGA, COPS3P1, 363 more genes
nsv4674043	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 165,010,461-190,957,473 , GRCh38.p12 chr4: 164,089,309-190,036,318	AGA, CYP4V2, 319 more genes
nsv3912039	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 164,039,530-189,982,708 , GRCh37 chr4: 164,960,682-190,828,225 , NCBI36 chr4: 165,180,132-191,140,857	AGA, CYP4V2, 314 more genes
nsv3916579	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,202,188-190,939,340 , GRCh38 chr4: 165,281,036-190,018,185 , NCBI36 chr4: 166,421,638-191,176,334	AGA, LOC105377614, 291 more genes
nsv4456171	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 166,623,890-190,957,473 , GRCh38.p12 chr4: 165,702,738-190,036,318	AGA, TRIML2, 284 more genes
nsv3913994	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 166,317,587-190,095,391 , GRCh37 chr4: 167,238,739-190,828,225 , NCBI36 chr4: 167,458,189-191,250,527	AGA, PTGES3P3, 290 more genes
nsv6634364	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318	AGA, LOC101928551, 279 more genes
nsv3918232	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 168,531,442-191,194,467 , GRCh37 chr4: 168,294,867-190,957,473 , GRCh38 chr4: 167,373,716-190,036,318	AGA, LOC105377560, 277 more genes
nsv3882557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 169,969,014-190,957,473 , GRCh38.p12 chr4: 169,047,863-190,036,318	AGA, LOC105377530, 258 more genes
nsv3921438	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 169,873,508-190,018,185 , NCBI36 chr4: 171,031,234-191,176,334 , GRCh37 chr4: 170,794,659-190,939,340	AGA, FAUP3, 245 more genes
nsv3886420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 162,205,710-182,329,883 , GRCh38.p12 chr4: 161,284,558-181,408,730	AGA, RPL35AP12, 187 more genes
nsv3914938	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 171,820,275-190,957,473 , NCBI36 chr4: 172,056,850-191,194,467 , GRCh38 chr4: 170,899,124-190,036,318	AGA, LOC112268472, 237 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 91

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Number of Variants: 20

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