pygm[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
nsv6309120	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,517,838-64,522,318 , GRCh38.p12 chr11: 64,750,366-64,754,846	PYGM
nsv6309375	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,514,121-64,518,065 , GRCh38.p12 chr11: 64,746,649-64,750,593	PYGM
nsv5672781	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,525,241-64,527,380 , GRCh38.p12 chr11: 64,757,769-64,759,908	PYGM
nsv4682158	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,525,698-64,526,196 , GRCh38.p12 chr11: 64,758,226-64,758,724	PYGM
nsv4683002	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,517,828-64,518,075 , GRCh38.p12 chr11: 64,750,356-64,750,603	PYGM
nsv4681693	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 64,517,838-64,518,065 , GRCh38.p12 chr11: 64,750,366-64,750,593	PYGM
nsv6315144	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 64,513,860-64,517,847 , GRCh38.p12 chr11: 64,746,388-64,750,375	PYGM
nsv4681676	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 64,514,111-64,514,850 , GRCh38.p12 chr11: 64,746,639-64,747,378	PYGM
nsv4681552	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 64,525,708-64,526,186 , GRCh38.p12 chr11: 64,758,236-64,758,714	PYGM
nsv7094176	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 64,520,525-64,523,631 , GRCh38.p12 chr11: 64,753,053-64,756,159	PYGM
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	PYGM, FAUP4, 2031 more genes
nsv6309121	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 64,522,783-66,283,694 , GRCh38.p12 chr11: 64,755,311-66,516,223	PYGM, SF3B2, 124 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	PYGM, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	PYGM, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	PYGM, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	PYGM, ATL3, 2125 more genes
nsv3902272	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 64,501,919-67,129,258 , GRCh38.p12 chr11: 64,734,447-67,361,787	PYGM, ACTN3, 157 more genes
nsv4436237	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 63,533,279-65,429,676 , GRCh38.p12 chr11: 63,765,807-65,662,205	PYGM, ARL2, 117 more genes
nsv4457218	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 64,474,135-64,611,928 , GRCh38.p12 chr11: 64,706,663-64,844,456	PYGM, CDC42BPG, 5 more genes
nsv7093694	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr11: 58,916,346-64,972,349 , GRCh38.p12 chr11: 59,148,873-65,204,878	PYGM, VPS37C, 298 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 22

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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