tacc3[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
nsv3918338	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr4: 1,694,954-1,761,799 , GRCh37 chr4: 1,725,156-1,792,001 , GRCh38 chr4: 1,723,429-1,790,274	TACC3, LOC112268460
nsv3883962	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr4: 1,735,761-1,806,926 , GRCh37 chr4: 1,737,488-1,808,653	TACC3, FGFR3, 1 more genes
nsv3877925	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,742,616-1,816,281 , GRCh38.p12 chr4: 1,740,889-1,814,554	TACC3, FGFR3, 2 more genes
nsv3881328	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 1,742,616-1,801,241 , GRCh38.p12 chr4: 1,740,889-1,799,514	TACC3, FGFR3, 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	TACC3, FAM53A, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, 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	TACC3, USP17L21, 318 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 146

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Number of Variants: 20

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