fam53a[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
nsv3879528	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,522,454-1,598,331 , GRCh38.p12 chr4: 1,520,727-1,596,604	FAM53A
nsv3885781	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,602,989-1,624,714 , GRCh38.p12 chr4: 1,601,262-1,622,987	FAM53A
nsv3882818	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,602,989-1,608,224 , GRCh38.p12 chr4: 1,601,262-1,606,497	FAM53A
nsv3885404	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,602,989-1,603,634 , GRCh38.p12 chr4: 1,601,262-1,601,907	FAM53A
nsv4454900	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,624,638-1,710,029 , GRCh38.p12 chr4: 1,622,911-1,708,302	FAM53A, SLBP, 1 more genes
nsv4452335	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,666,159-1,738,239 , GRCh38.p12 chr4: 1,664,432-1,736,512	FAM53A, TMEM129, 2 more genes
nsv4452470	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,684,415-1,764,940 , GRCh38.p12 chr4: 1,682,688-1,763,213	FAM53A, LOC112268460, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, 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	FAM53A, RN7SL589P, 323 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 149

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Number of Variants: 20

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