alg11[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
nsv6314657	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr13: 52,549,305-52,585,631 , GRCh38.p12 chr13: 51,975,169-52,011,495	ALG11, ATP7B
nsv4681298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 52,508,882-52,603,794 , GRCh38.p12 chr13: 51,934,746-52,029,658	ALG11, ATP7B, 2 more genes
nsv4681170	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 52,508,872-52,602,746 , GRCh38.p12 chr13: 51,934,736-52,028,610	ALG11, FABP5P2, 2 more genes
nsv7094084	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 52,508,892-52,585,473 , GRCh38.p12 chr13: 51,934,756-52,011,337	ALG11, FABP5P2, 1 more genes
nsv4681285	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 52,585,413-52,603,794 , GRCh38.p12 chr13: 52,011,277-52,029,658	ALG11, ATP7B, 1 more genes
nsv5672653	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr13: 52,585,403-52,602,726 , GRCh38.p12 chr13: 52,011,267-52,028,590	ALG11, ATP7B, 1 more genes
nsv3901272	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr13: 52,580,525-52,693,303 , GRCh38.p12 chr13: 52,006,389-52,119,167	ALG11, ATP7B, 2 more genes
nsv3871961	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr13: 51,964,852-52,028,610 , GRCh37 chr13: 52,538,988-52,602,746	ALG11, UTP14C, 2 more genes
nsv6309683	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 52,538,988-52,585,473 , GRCh38.p12 chr13: 51,964,852-52,011,337	ALG11, FABP5P2, 1 more genes
nsv3910270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 18,445,862-114,327,173 , NCBI36 chr13: 10,098,739-114,110,750 , GRCh37 chr13: 19,020,001-115,085,141	ALG11, RNU6-71P, 1332 more genes
nsv3924528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 41,516,434-115,085,141 , GRCh38 chr13: 40,942,298-114,340,331 , NCBI36 chr13: 40,414,434-114,123,908	ALG11, LOC105370271, 925 more genes
nsv3898603	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 42,457,841-91,796,698 , GRCh38.p12 chr13: 41,883,705-91,144,444	ALG11, RNY4P30, 575 more genes
nsv3918812	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 44,967,523-92,738,168 , NCBI36 chr13: 44,439,658-92,188,422 , GRCh37 chr13: 45,541,658-93,390,421	ALG11, SRSF1P1, 541 more genes
nsv6314117	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618	ALG11, RBM26, 591 more genes
nsv3913649	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 41,143,820-85,137,552 , GRCh37 chr13: 41,717,956-85,711,687 , NCBI36 chr13: 40,615,956-84,609,688	ALG11, RPL21P108, 539 more genes
nsv3882264	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 46,968,080-87,381,985 , GRCh37.p13 chr13: 47,542,215-88,034,240	ALG11, ARL11, 428 more genes
nsv4675995	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 51,512,603-91,631,111 , GRCh38.p12 chr13: 50,938,467-90,978,857	ALG11, RNU7-88P, 396 more genes
nsv3915679	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 31,271,865-70,046,105 , GRCh38 chr13: 30,697,728-69,471,973 , NCBI36 chr13: 30,169,865-68,944,106	ALG11, CCDC70, 524 more genes
nsv3915859	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 47,117,587-84,300,935 , GRCh37 chr13: 47,691,722-84,875,070 , NCBI36 chr13: 46,589,723-83,773,071	ALG11, LOC105370231, 406 more genes
nsv3923911	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 38,438,363-68,537,920 , GRCh38 chr13: 37,864,226-67,963,788 , NCBI36 chr13: 37,336,363-67,435,921	ALG11, MLNR, 422 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 68

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Number of Variants: 20

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