DEPDC5 - 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
nsv3871239	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 32,154,512-32,174,174 , GRCh38.p12 chr22: 31,758,526-31,778,188	DEPDC5
nsv6636172	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,188,813-32,205,587 , GRCh38.p12 chr22: 31,792,827-31,809,601	DEPDC5
nsv7095939	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,179,873-32,193,709 , GRCh38.p12 chr22: 31,783,887-31,797,723	DEPDC5
nsv5673433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,174,065-32,180,881 , GRCh38.p12 chr22: 31,778,079-31,784,895	DEPDC5
nsv7148139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,174,085-32,180,861 , GRCh38.p12 chr22: 31,778,099-31,784,875	DEPDC5
nsv5673279	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,188,019-32,194,642 , GRCh38.p12 chr22: 31,792,033-31,798,656	DEPDC5
nsv4450064	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 32,200,128-32,206,647 , GRCh38 chr22: 31,804,142-31,810,661	DEPDC5
nsv3871609	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 31,809,591-31,815,232 , GRCh37 chr22: 32,205,577-32,211,218	DEPDC5
nsv6311127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,188,404-32,191,244 , GRCh38.p12 chr22: 31,792,418-31,795,258	DEPDC5
nsv7096306	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,239,061-32,241,243 , GRCh38.p12 chr22: 31,843,075-31,845,257	DEPDC5
nsv4453617	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 32,160,941-32,162,674 , GRCh38 chr22: 31,764,955-31,766,688	DEPDC5
nsv7096349	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,193,566-32,194,662 , GRCh38.p12 chr22: 31,797,580-31,798,676	DEPDC5
nsv5673280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,205,577-32,206,647 , GRCh38.p12 chr22: 31,809,591-31,810,661	DEPDC5
nsv7096305	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,187,999-32,188,823 , GRCh38.p12 chr22: 31,792,013-31,792,837	DEPDC5
nsv7095827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,239,061-32,239,818 , GRCh38.p12 chr22: 31,843,075-31,843,832	DEPDC5
nsv7095829	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,301,950-32,302,483 , GRCh38.p12 chr22: 31,905,964-31,906,497	DEPDC5
nsv5673434	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,301,960-32,302,483 , GRCh38.p12 chr22: 31,905,974-31,906,497	DEPDC5
nsv7096351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,234,651-32,234,851 , GRCh38.p12 chr22: 31,838,665-31,838,865	DEPDC5
nsv3877564	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr22: 31,758,526-31,758,653 , GRCh37 chr22: 32,154,512-32,154,639	DEPDC5
nsv5673195	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 32,160,941-32,161,066 , GRCh38.p12 chr22: 31,764,955-31,765,080	DEPDC5

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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

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Items: 1 to 20 of 524

Page of 27

Number of Variants: 20

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