bmpr2[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
nsv3881710	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 202,377,474-202,514,887 , GRCh37 chr2: 203,242,197-203,379,610	BMPR2
nsv3881069	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,242,197-203,378,441 , GRCh38 chr2: 202,377,474-202,513,718	BMPR2
nsv3881297	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 202,376,935-202,464,808 , GRCh37 chr2: 203,241,658-203,329,531	BMPR2
nsv3876077	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,242,197-203,329,531 , GRCh38 chr2: 202,377,474-202,464,808	BMPR2
nsv6311366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,329,522-203,379,712 , GRCh38.p12 chr2: 202,464,799-202,514,989	BMPR2
nsv3883753	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 203,332,222-203,379,722 , GRCh38 chr2: 202,467,499-202,514,999	BMPR2
nsv3887007	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,407,171-203,424,670 , GRCh38 chr2: 202,542,448-202,559,947	BMPR2
nsv4681504	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 203,395,507-203,407,180 , GRCh38.p12 chr2: 202,530,784-202,542,457	BMPR2
nsv5060006	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,234,119-203,242,446 , GRCh38 chr2: 202,369,396-202,377,723	BMPR2
nsv5673363	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 202,373,246-202,381,016 , GRCh37 chr2: 203,237,969-203,245,739	BMPR2
nsv5673443	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,325,958-203,332,529 , GRCh38 chr2: 202,461,235-202,467,806	BMPR2
nsv5673445	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,406,743-203,411,905 , GRCh38 chr2: 202,542,020-202,547,182	BMPR2
nsv5673455	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,329,512-203,332,432 , GRCh38.p12 chr2: 202,464,789-202,467,709	BMPR2
nsv3872453	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 202,464,809-202,467,689 , GRCh37 chr2: 203,329,532-203,332,412	BMPR2
nsv7096226	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,378,422-203,379,722 , GRCh38.p12 chr2: 202,513,699-202,514,999	BMPR2
nsv5673688	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,378,432-203,379,712 , GRCh38.p12 chr2: 202,513,709-202,514,989	BMPR2
nsv5673214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,241,529-203,242,283 , GRCh38.p12 chr2: 202,376,806-202,377,560	BMPR2
nsv7096124	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,332,222-203,332,432 , GRCh38.p12 chr2: 202,467,499-202,467,709	BMPR2
nsv3888719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 203,242,135-203,242,334 , GRCh38 chr2: 202,377,412-202,377,611	BMPR2
nsv4682022	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 203,332,232-203,332,422 , GRCh38.p12 chr2: 202,467,509-202,467,699	BMPR2

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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 101

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Number of Variants: 20

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Supplemental Content

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