fgfbp2[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
nsv3924433	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr4: 15,407,092-15,673,330 , GRCh37 chr4: 15,797,994-16,064,232 , GRCh38 chr4: 15,796,371-16,062,609	FGFBP2, PROM1, 3 more genes
nsv4729453	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 15,940,736-16,004,666 , GRCh38.p12 chr4: 15,939,113-16,003,043	FGFBP2, PROM1, 1 more genes
nsv5381429	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 15,964,081-16,172,352 , GRCh38.p12 chr4: 15,962,458-16,170,729	FGFBP2, LOC105374502, 3 more genes
nsv3877950	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 4,165,334-33,324,781 , GRCh38.p12 chr4: 4,163,607-33,323,159	FGFBP2, LOC100418700, 353 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	FGFBP2, 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	FGFBP2, OR7E99P, 446 more genes
nsv7098818	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 11,399,082-38,137,335 , GRCh37.p13 chr4: 11,400,706-38,138,956	FGFBP2, LOC105374542, 232 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, 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	FGFBP2, RPS3AP16, 332 more genes
nsv4347528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,778,849-27,760,141 , GRCh38.p12 chr4: 12,777,225-27,758,519	FGFBP2, MTCO3P44, 148 more genes
nsv3917447	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 4,479,031-17,071,270 , GRCh38 chr4: 4,426,403-17,460,549 , GRCh37 chr4: 4,428,130-17,462,172	FGFBP2, SNORD162, 218 more genes
nsv3922899	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr4: 13,671,851-19,732,555 , GRCh37 chr4: 14,062,753-20,123,457 , GRCh38 chr4: 14,061,129-20,121,834	FGFBP2, CD38, 58 more genes
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	FGFBP2, LOC100422029, 2358 more genes

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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 54

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Number of Variants: 20

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