vegfc[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
nsv4456383	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr4: 177,590,756-177,695,769 , GRCh38.p12 chr4: 176,669,605-176,774,615	VEGFC, HAFML
nsv3880694	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 177,605,840-177,851,556 , GRCh38.p12 chr4: 176,684,686-176,930,402	VEGFC, LINC02509, 1 more genes
nsv3876482	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 177,342,830-177,869,978 , GRCh38.p12 chr4: 176,421,679-176,948,824	VEGFC, LOC100421630, 2 more genes
nsv3884346	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 177,194,007-177,710,725 , GRCh38.p12 chr4: 176,272,856-176,789,571	VEGFC, ASB5, 3 more genes
nsv3913826	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 177,425,113-177,933,663 , GRCh37.p13 chr4: 177,188,119-177,696,669 , GRCh38.p12 chr4: 176,266,968-176,775,515	VEGFC, HAFML, 3 more genes
nsv6291006	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 177,188,481-177,619,344 , GRCh38.p12 chr4: 176,267,330-176,698,190	VEGFC, HAFML, 3 more genes
nsv3876324	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 177,242,181-177,649,158 , GRCh38.p12 chr4: 176,321,030-176,728,004	VEGFC, LOC100421630, 2 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, 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	VEGFC, LOC132386, 224 more genes

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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 80

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Number of Variants: 20

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