fbxo8[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
nsv3870597	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 175,150,481-175,240,518 , GRCh38.p12 chr4: 174,229,330-174,319,367	FBXO8, CEP44
nsv4456798	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 174,991,467-175,194,923 , GRCh38.p12 chr4: 174,070,316-174,273,772	FBXO8, LINC02268, 1 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, 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	FBXO8, LOC112268472, 237 more genes
nsv4348053	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 171,663,620-190,431,429 , GRCh38.p12 chr4: 170,742,469-189,510,275	FBXO8, LOC132386, 224 more genes
nsv3913296	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 172,665,430-191,027,875 , GRCh38 chr4: 171,507,704-189,869,726 , GRCh37 chr4: 172,428,855-190,790,881	FBXO8, LINC02434, 223 more genes
nsv3916987	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 169,891,551-187,857,892 , GRCh38 chr4: 168,970,400-186,936,738 , NCBI36 chr4: 170,128,126-188,094,886	FBXO8, LINC02500, 210 more genes
nsv3914027	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 172,356,988-189,975,519 , NCBI36 chr4: 173,514,714-191,133,668 , GRCh37 chr4: 173,278,139-190,828,225	FBXO8, LINC02374, 223 more genes
nsv3910075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 173,422,525-190,828,225 , NCBI36 chr4: 173,659,100-191,250,468 , GRCh38 chr4: 172,501,374-190,095,332	FBXO8, LOC112268472, 239 more genes
nsv6315348	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318	FBXO8, SPATA4, 203 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 69

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Number of Variants: 20

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