mxd4[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
nsv3877210	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,572-2,264,421 , GRCh38.p12 chr4: 2,261,845-2,262,694	MXD4
nsv3871725	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,139-2,264,421 , GRCh38.p12 chr4: 2,261,412-2,262,694	MXD4
nsv3885830	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,153-2,264,421 , GRCh38.p12 chr4: 2,261,426-2,262,694	MXD4
nsv3879141	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,469-2,264,421 , GRCh38.p12 chr4: 2,261,742-2,262,694	MXD4
nsv3879921	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,572-2,270,534 , GRCh38.p12 chr4: 2,261,845-2,268,807	MXD4, ZFYVE28
nsv3878771	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,250,109-2,264,421 , GRCh38.p12 chr4: 2,248,382-2,262,694	MXD4, MIR4800
nsv3887436	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,261,720-2,270,534 , GRCh38.p12 chr4: 2,259,993-2,268,807	MXD4, ZFYVE28
nsv3886862	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,139-2,270,534 , GRCh38.p12 chr4: 2,261,412-2,268,807	MXD4, ZFYVE28
nsv3873502	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,263,153-2,270,534 , GRCh38.p12 chr4: 2,261,426-2,268,807	MXD4, ZFYVE28
nsv3886622	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,250,109-2,275,145 , GRCh38.p12 chr4: 2,248,382-2,273,418	MXD4, MIR4800, 1 more genes
nsv3885103	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,233,709-2,261,720 , GRCh38.p12 chr4: 2,231,982-2,259,993	MXD4, COX6B1P5, 3 more genes
nsv3881991	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 2,233,709-2,252,881 , GRCh38.p12 chr4: 2,231,982-2,251,154	MXD4, MIR4800, 3 more genes
nsv3885762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-29,006,745 , GRCh38.p12 chr4: 71,660-29,005,123	MXD4, CD38, 456 more genes
nsv3923296	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-28,066,309 , NCBI36 chr4: 62,447-27,677,029 , GRCh37 chr4: 72,447-28,067,931	MXD4, OR7E99P, 446 more genes
nsv4674378	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-24,280,482 , GRCh38.p12 chr4: 49,556-24,278,859	MXD4, USP17L30, 394 more genes
nsv6315347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952	MXD4, LOC100421802, 375 more genes
nsv6291097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,587,167 , GRCh38.p12 chr4: 68,453-20,585,544	MXD4, LOC105374479, 372 more genes
nsv3915161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,387,231 , NCBI36 chr4: 58,345-19,996,329 , GRCh38 chr4: 68,453-20,385,608	MXD4, CTBP1-AS, 370 more genes
nsv1398080	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,020-19,796,182 , GRCh38.p12 chr4: 44,019-19,794,559	MXD4, RPL10AP7, 366 more genes
nsv6112747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,598-18,912,995 , GRCh38.p12 chr4: 68,706-18,911,372	MXD4, GPR78, 362 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 142

Page of 8

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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