hand2[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
nsv3881926	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 174,447,767-174,457,917 , GRCh38.p12 chr4: 173,526,616-173,536,766	HAND2-AS1, HAND2
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	COPS3P1, LOC339975, 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	CYP4V2, ZFP42, 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	CYP4V2, IRF2, 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	LOC105377614, TRAPPC11, 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	TRIML2, LTO1P1, 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	PTGES3P3, LOC105377523, 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	LOC101928551, LOC107986330, 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	LOC105377560, LOC105377563, 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	LOC105377530, LOC105377613, 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	FAUP3, LOC107986328, 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	RPL35AP12, LOC107986326, 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	LOC112268472, FRG1-DT, 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	LOC132386, DCTD, 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	LINC02434, LOC105377603, 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	LINC02500, TENM3-AS1, 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	LINC02374, RANP6, 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	LOC112268472, KLKB1, 239 more genes
nsv4729375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 169,108,358-184,425,536 , GRCh38.p12 chr4: 168,187,207-183,504,383	GALNT7-DT, LOC105377524, 154 more genes
nsv3878182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 162,344,510-177,103,037 , GRCh38.p12 chr4: 161,423,358-176,181,886	LINC02504, GLRA3, 156 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 64

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Number of Variants: 20

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