mgat4c[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
nsv3899668	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,422,840-86,485,493 , GRCh38.p12 chr12: 86,029,062-86,091,715	MGAT4C
nsv3909734	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,384,306-86,431,985 , GRCh38.p12 chr12: 85,990,528-86,038,207	MGAT4C
nsv3902363	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,393,513-86,432,225 , GRCh38.p12 chr12: 85,999,735-86,038,447	MGAT4C
nsv3908717	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,393,513-86,431,985 , GRCh38.p12 chr12: 85,999,735-86,038,207	MGAT4C
nsv3899820	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,393,513-86,428,947 , GRCh38.p12 chr12: 85,999,735-86,035,169	MGAT4C
nsv3902006	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,673,989-86,703,959 , GRCh38.p12 chr12: 86,280,211-86,310,181	MGAT4C
nsv3907228	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,408,570-86,431,985 , GRCh38.p12 chr12: 86,014,792-86,038,207	MGAT4C
nsv3898916	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,695,712-86,707,643 , GRCh38.p12 chr12: 86,301,934-86,313,865	MGAT4C
nsv3898981	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 87,204,748-87,216,285 , GRCh38.p12 chr12\|NW_015148967.1: 42,762-54,299 , GRCh38.p12 chr12: 86,810,971-86,822,508	MGAT4C
nsv3904346	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,695,712-86,702,906 , GRCh38.p12 chr12: 86,301,934-86,309,128	MGAT4C
nsv4729539	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 86,432,529-86,529,656 , GRCh38.p12 chr12: 86,038,751-86,135,878	MGAT4C
nsv4456770	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 86,438,504-86,522,229 , GRCh38.p12 chr12: 86,044,726-86,128,451	MGAT4C
nsv3910372	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 85,490,387-85,799,399 , GRCh37 chr12: 86,966,256-87,275,268 , GRCh38 chr12: 86,572,479-86,881,491	MGAT4C, MIR3059
nsv3903573	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,650,365-86,702,906 , GRCh38.p12 chr12: 86,256,587-86,309,128	MGAT4C, LOC105369877
nsv3895134	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,673,989-87,274,871 , GRCh38.p12 chr12: 86,280,211-86,881,094	MGAT4C, MIR3059
nsv3901527	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,695,712-87,281,219 , GRCh38.p12 chr12: 86,301,934-86,887,442	MGAT4C, MIR3059
nsv3898372	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 86,697,806-87,281,219 , GRCh38.p12 chr12: 86,304,028-86,887,442	MGAT4C, MIR3059
nsv3923900	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 85,347,260-86,245,369 , GRCh37 chr12: 86,823,129-87,721,238 , GRCh38 chr12: 86,429,352-87,327,461	MGAT4C, MIR3059, 2 more genes
nsv3895887	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 87,188,645-87,582,711 , GRCh38.p12 chr12: 86,794,868-87,188,934 , GRCh38.p12 chr12\|NW_015148967.1: 26,659-315,610	MGAT4C, RPL23AP68, 1 more genes
nsv3921905	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr12: 85,731,374-86,102,504 , GRCh37 chr12: 87,207,243-87,578,373 , GRCh38 chr12: 86,813,466-87,184,596	MGAT4C, LOC105369878, 1 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 44

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Number of Variants: 20

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