dbVar for Gene (Select 493860) - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Location	Genes in region
nsv7142942	insertion	1	nstd232	human	GRCh37.p13 chr11: 32,777,440-32,777,440 , GRCh38.p12 chr11: 32,755,894-32,755,894	CCDC73
nsv7139432	copy number variation	1	nstd232	human	GRCh37.p13 chr11: 32,777,215-32,777,294 , GRCh38.p12 chr11: 32,755,669-32,755,748	CCDC73
nsv7077680	inversion	1	nstd229	human	GRCh38 chr11: 32,729,441-32,729,551 , GRCh37.p13 chr11: 32,750,987-32,751,097	CCDC73
nsv7069630	inversion	1	nstd229	human	GRCh38 chr11: 32,759,344-32,764,295 , GRCh37.p13 chr11: 32,780,890-32,785,841	CCDC73
nsv6917964	copy number variation	1	nstd229	human	GRCh38 chr11: 32,700,318-32,704,081 , GRCh37.p13 chr11: 32,721,864-32,725,627	CCDC73
nsv6917624	copy number variation	1	nstd229	human	GRCh38 chr11: 32,749,301-32,752,300 , GRCh37.p13 chr11: 32,770,847-32,773,846	CCDC73
nsv6916961	copy number variation	1	nstd229	human	GRCh38 chr11: 32,749,239-32,749,327 , GRCh37.p13 chr11: 32,770,785-32,770,873	CCDC73
nsv6916002	copy number variation	1	nstd229	human	GRCh38 chr11: 32,687,350-32,748,254 , GRCh37.p13 chr11: 32,708,896-32,769,800	CCDC73
nsv6915225	copy number variation	1	nstd229	human	GRCh38 chr11: 32,636,639-32,676,909 , GRCh37.p13 chr11: 32,658,185-32,698,455	CCDC73
nsv6914672	copy number variation	1	nstd229	human	GRCh38 chr11: 32,671,451-32,771,201 , GRCh37.p13 chr11: 32,692,997-32,792,747	RPL34P2, CCDC73
nsv6914302	copy number variation	1	nstd229	human	GRCh38 chr11: 32,638,777-32,639,244 , GRCh37.p13 chr11: 32,660,323-32,660,790	CCDC73
nsv6913658	copy number variation	1	nstd229	human	GRCh38 chr11: 32,667,622-32,702,181 , GRCh37.p13 chr11: 32,689,168-32,723,727	CCDC73
nsv6913650	copy number variation	1	nstd229	human	GRCh38 chr11: 32,731,501-32,747,300 , GRCh37.p13 chr11: 32,753,047-32,768,846	CCDC73
nsv6913070	copy number variation	1	nstd229	human	GRCh38 chr11: 32,707,901-32,716,300 , GRCh37.p13 chr11: 32,729,447-32,737,846	CCDC73
nsv6911402	copy number variation	1	nstd229	human	GRCh38 chr11: 32,673,335-32,764,618 , GRCh37.p13 chr11: 32,694,881-32,786,164	CCDC73, RPL34P2
nsv6910950	copy number variation	1	nstd229	human	GRCh38 chr11: 32,732,273-32,816,726 , GRCh37.p13 chr11: 32,753,819-32,838,272	CCDC73, RPL34P2
nsv6910296	copy number variation	1	nstd229	human	GRCh38 chr11: 32,781,817-32,782,379 , GRCh37.p13 chr11: 32,803,363-32,803,925	CCDC73
nsv6909180	copy number variation	1	nstd229	human	GRCh38 chr11: 32,666,811-32,686,939 , GRCh37.p13 chr11: 32,688,357-32,708,485	CCDC73
nsv6908990	copy number variation	1	nstd229	human	GRCh38 chr11: 32,710,956-32,719,550 , GRCh37.p13 chr11: 32,732,502-32,741,096	CCDC73
nsv6907043	copy number variation	1	nstd229	human	GRCh38 chr11: 32,667,024-32,678,845 , GRCh37.p13 chr11: 32,688,570-32,700,391	CCDC73

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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

Links from Gene

Items: 1 to 20 of 642

Page of 33

Number of Variants: 20

Page of 33

Supplemental Content

Find related data

Recent activity