abat[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
nsv7094700	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 8,839,838-8,870,367 , GRCh38.p12 chr16: 8,745,981-8,776,510	ABAT
nsv6309887	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 8,844,259-8,875,287 , GRCh38.p12 chr16: 8,750,402-8,781,430	ABAT
nsv7137098	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 8,841,965-8,851,663 , GRCh38.p12 chr16: 8,748,108-8,757,806	ABAT
nsv6310021	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 8,851,594-8,862,850 , GRCh38.p12 chr16: 8,757,737-8,768,993	ABAT
nsv7095053	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,857,906-8,862,850 , GRCh38.p12 chr16: 8,764,049-8,768,993	ABAT
nsv6310100	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,857,906-8,858,707 , GRCh38.p12 chr16: 8,764,049-8,764,850	ABAT
nsv4681976	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,857,916-8,875,287 , GRCh38.p12 chr16: 8,764,059-8,781,430	ABAT
nsv7094609	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,873,316-8,875,287 , GRCh38.p12 chr16: 8,779,459-8,781,430	ABAT
nsv3890919	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 8,811,986-8,839,954 , GRCh38.p12 chr16: 8,718,129-8,746,097	ABAT, LOC107984840
nsv4453434	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr16: 8,735,720-8,781,450 , GRCh37 chr16: 8,829,577-8,875,307	ABAT, LOC107984840
nsv7095109	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,875,287 , GRCh38.p12 chr16: 8,735,740-8,781,430	ABAT, LOC107984840
nsv6309935	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,862,850 , GRCh38.p12 chr16: 8,735,740-8,768,993	ABAT, LOC107984840
nsv7095108	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,858,707 , GRCh38.p12 chr16: 8,735,740-8,764,850	ABAT, LOC107984840
nsv6309934	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,844,416 , GRCh38.p12 chr16: 8,735,740-8,750,559	ABAT, LOC107984840
nsv7095107	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,839,975 , GRCh38.p12 chr16: 8,735,740-8,746,118	ABAT, LOC107984840
nsv7095051	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,829,686 , GRCh38.p12 chr16: 8,735,740-8,735,829	ABAT, LOC107984840
nsv5564149	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 8,829,597-8,829,676 , GRCh38.p12 chr16: 8,735,740-8,735,819	ABAT, LOC107984840
nsv4451596	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 8,873,316-8,941,702 , GRCh38 chr16: 8,779,459-8,847,845	ABAT, TMEM186, 2 more genes
nsv3902217	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 8,722,052-8,875,529 , GRCh38.p12 chr16: 8,628,195-8,781,672	ABAT, RNU7-63P, 3 more genes
nsv3898679	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr16: 8,861,856-8,891,690 , GRCh38.p12 chr16: 8,767,999-8,797,833	ABAT, TMEM186, 1 more genes

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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 112

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Number of Variants: 20

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