maea[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
nsv3910141	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr4: 1,330,963-1,348,155 , NCBI36 chr4: 1,314,751-1,331,943 , GRCh37 chr4: 1,324,751-1,341,943	MAEA, UVSSA
nsv3921140	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr4: 1,314,751-1,354,014 , GRCh37 chr4: 1,324,751-1,364,014 , GRCh38 chr4: 1,330,963-1,370,226	MAEA, UVSSA
nsv3881096	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,281,951-1,290,436 , GRCh38.p12 chr4: 1,288,163-1,296,648	MAEA, LOC105374347, 1 more genes
nsv3924093	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr4: 1,234,663-1,330,963 , GRCh37 chr4: 1,228,451-1,324,751 , NCBI36 chr4: 1,218,451-1,314,751	MAEA, LOC105374347, 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	MAEA, 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	MAEA, 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	MAEA, 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	MAEA, 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	MAEA, 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	MAEA, 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	MAEA, 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	MAEA, GPR78, 362 more genes
nsv3915014	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 75,040-17,097,463 , GRCh38 chr4: 85,149-17,486,742 , GRCh37 chr4: 85,040-17,488,365	MAEA, LOC100422637, 350 more genes
nsv3915275	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 72,447-17,279,636 , GRCh38 chr4: 72,555-17,278,013 , NCBI36 chr4: 62,447-16,888,734	MAEA, OR7E99P, 347 more genes
nsv3888069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-15,973,383 , GRCh38.p12 chr4: 68,453-15,971,760	MAEA, RPS3AP16, 332 more genes
nsv3917860	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 37,335-15,869,056 , NCBI36 chr4: 27,336-15,479,777 , GRCh37 chr4: 37,336-15,870,679	MAEA, LOC105374338, 330 more genes
nsv3918310	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 72,555-15,658,035 , GRCh37 chr4: 72,447-15,659,658 , NCBI36 chr4: 62,447-15,268,756	MAEA, RN7SL589P, 323 more genes
nsv3887204	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 71,552-15,302,739 , GRCh38.p12 chr4: 71,660-15,301,115	MAEA, USP17L21, 318 more genes
nsv3911947	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-14,614,077 , NCBI36 chr4: 58,345-14,223,175 , GRCh38 chr4: 68,453-14,612,453	MAEA, MIR572, 313 more genes
nsv3914961	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 46,772-14,110,482 , GRCh38 chr4: 56,878-14,499,760 , GRCh37 chr4: 56,772-14,501,384	MAEA, LOC101928532, 311 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 144

Page of 8

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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