atg13[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
nsv3898416	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,560,809-46,720,908 , GRCh38.p12 chr11: 46,539,259-46,699,358	ATG13, AMBRA1, 3 more genes
nsv3875730	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,582,062-46,725,972 , GRCh38 chr11: 46,560,512-46,704,422	ATG13, ARHGAP1, 3 more genes
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	ATG13, FAUP4, 2031 more genes
nsv3922177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947	ATG13, MIR3160-2, 122 more genes
nsv3913842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735	ATG13, MIR3160-1, 162 more genes
nsv3924778	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131	ATG13, F2, 140 more genes
nsv6291196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167	ATG13, LINC02687, 86 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	ATG13, 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	ATG13, 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	ATG13, 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	ATG13, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	ATG13, TRR-TCT3-2, 494 more genes
nsv5380725	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218	ATG13, MIR4688, 58 more genes
nsv3914563	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735	ATG13, ACP2, 143 more genes
nsv6313964	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,248,477-46,748,132 , GRCh38.p12 chr11: 46,226,926-46,726,582	ATG13, ARHGAP1, 13 more genes
nsv4729636	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,418,839-46,753,136 , GRCh38.p12 chr11: 46,397,289-46,731,586	ATG13, MIR3160-2, 7 more genes
nsv3924490	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr11: 46,399,081-46,706,498 , GRCh38 chr11: 46,420,955-46,728,372 , GRCh37 chr11: 46,442,505-46,749,922	ATG13, ARHGAP1, 7 more genes
nsv3907110	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,502,259-46,745,473 , GRCh38.p12 chr11: 46,480,709-46,723,923	ATG13, ARHGAP1, 4 more genes
nsv5380726	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,569,796-46,742,390 , GRCh38.p12 chr11: 46,548,246-46,720,840	ATG13, AMBRA1, 4 more genes
nsv4456633	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,302,171-46,783,079 , GRCh38.p12 chr11: 46,280,620-46,761,529	ATG13, MIR5582, 15 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 23

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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