bmpr1a[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
nsv7093896	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,676,881-88,683,476 , GRCh38.p12 chr10: 86,917,124-86,923,719	BMPR1A
nsv3886697	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 88,671,987-88,677,093 , GRCh38 chr10: 86,912,230-86,917,336	BMPR1A
nsv7093738	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,676,881-88,679,236 , GRCh38.p12 chr10: 86,917,124-86,919,479	BMPR1A
nsv7093739	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,683,123-88,683,476 , GRCh38.p12 chr10: 86,923,366-86,923,719	BMPR1A
nsv6309012	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,659,541-88,659,893 , GRCh38.p12 chr10: 86,899,784-86,900,136	BMPR1A
nsv6309086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,678,919-88,679,236 , GRCh38.p12 chr10: 86,919,162-86,919,479	BMPR1A
nsv4683006	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr10: 88,635,625-88,635,852 , GRCh38.p12 chr10: 86,875,868-86,876,095	BMPR1A
nsv5672765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr10: 88,651,874-88,651,996 , GRCh38.p12 chr10: 86,892,117-86,892,239	BMPR1A
nsv4451427	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr10: 86,876,009-86,876,095 , GRCh37 chr10: 88,635,766-88,635,852	BMPR1A
nsv6290154	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 88,659,884-88,681,276 , GRCh38.p12 chr10: 86,900,127-86,921,519	BMPR1A
nsv5672533	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr10: 88,671,987-88,683,476 , GRCh38.p12 chr10: 86,912,230-86,923,719	BMPR1A
nsv4682749	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr10: 88,671,987-88,679,236 , GRCh38.p12 chr10: 86,912,230-86,919,479	BMPR1A
nsv3871807	copy number variation	2	nstd102	human	Uncertain significance, Likely pathogenic	GRCh37 chr10: 88,598,623-88,603,267 , GRCh38 chr10: 86,838,866-86,843,510	BMPR1A
nsv3879263	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr10: 88,514,773-88,516,802 , GRCh38 chr10: 86,755,016-86,757,045	BMPR1A
nsv4453625	copy number variation	2	nstd102	human	Likely pathogenic	GRCh37 chr10: 88,514,773-88,516,676 , GRCh38 chr10: 86,755,016-86,756,919	BMPR1A
nsv4681201	copy number variation	2	nstd102	human	Uncertain significance, Likely pathogenic	GRCh37 chr10: 88,598,623-88,598,738 , GRCh38.p12 chr10: 86,838,866-86,838,981	BMPR1A
nsv3907477	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 88,516,121-88,520,409 , GRCh38.p12 chr10: 86,756,364-86,760,652	BMPR1A
nsv3891753	copy number variation	1	nstd102	human	Benign	GRCh37 chr10: 88,516,121-88,516,768 , GRCh38.p12 chr10: 86,756,364-86,757,011	BMPR1A
nsv5564366	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 88,514,773-88,598,738 , GRCh38.p12 chr10: 86,755,016-86,838,981	BMPR1A
nsv4454099	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr10: 88,659,541-88,683,486 , GRCh38 chr10: 86,899,784-86,923,729	BMPR1A

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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 110

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Number of Variants: 20

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