atg5[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
nsv4674848	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 106,427,169-106,641,115 , GRCh38.p12 chr6: 105,979,294-106,193,240	ATG5, PRDM1
nsv6314604	complex chromosomal rearrangement	8	nstd102	human	Pathogenic	GRCh37 chr2: 200,268,602-200,268,602 , GRCh37 chr2: 200,277,100-200,277,100 , GRCh37 chr2: 200,306,110-200,306,110 , GRCh37 chr2: 200,356,046-200,356,046 , GRCh37 chr6: 102,551,327-102,551,327 , GRCh37 chr6: 102,554,425-102,554,425 , GRCh37 chr6: 102,933,427-102,933,427 , GRCh37 chr6: 102,933,469-102,933,469 , GRCh37 chr6: 106,681,471-106,681,471 , GRCh37 chr6: 106,704,624-106,704,624 , GRCh37 chr6: 107,030,770-107,030,770 , GRCh37 chr6: 107,030,770-107,030,770 , GRCh37 chr6: 107,167,239-107,167,239 , GRCh37 chr6: 107,168,609-107,168,609 , GRCh37 chr6: 107,170,741-107,170,741 , GRCh37 chr6: 107,170,881-107,170,881 , GRCh38.p12 chr2: 199,403,879-199,403,879 , GRCh38.p12 chr2: 199,412,377-199,412,377 , GRCh38.p12 chr2: 199,441,387-199,441,387 , GRCh38.p12 chr2: 199,491,323-199,491,323 , GRCh38.p12 chr6: 102,103,452-102,103,452 , GRCh38.p12 chr6: 102,106,550-102,106,550 , GRCh38.p12 chr6: 102,485,552-102,485,552 , GRCh38.p12 chr6: 102,485,594-102,485,594 , GRCh38.p12 chr6: 106,233,596-106,233,596 , GRCh38.p12 chr6: 106,256,749-106,256,749 , GRCh38.p12 chr6: 106,582,895-106,582,895 , GRCh38.p12 chr6: 106,582,895-106,582,895 , GRCh38.p12 chr6: 106,719,364-106,719,364 , GRCh38.p12 chr6: 106,720,734-106,720,734 , GRCh38.p12 chr6: 106,722,866-106,722,866 , GRCh38.p12 chr6: 106,723,006-106,723,006	ATG5, SATB2, 2 more genes
nsv4729692	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 106,330,947-106,730,123 , GRCh38.p12 chr6: 105,883,072-106,282,248	ATG5, RN7SKP211, 3 more genes
nsv3880626	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 85,988,428-120,548,687 , GRCh38.p12 chr6: 85,278,710-120,227,541	ATG5, LOC107986534, 426 more genes
nsv6313858	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488	ATG5, RN7SL509P, 311 more genes
nsv3924576	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,164,591-122,524,393 , GRCh38 chr6: 96,609,994-122,161,548 , GRCh37 chr6: 97,057,870-122,482,694	ATG5, TUBE1, 318 more genes
nsv3876958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 95,549,951-116,684,929 , GRCh38.p12 chr6: 94,840,233-116,363,766	ATG5, LIN28B-AS1, 258 more genes
nsv3910417	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 100,054,889-120,488,154 , NCBI36 chr6: 100,609,486-120,850,999 , GRCh37 chr6: 100,502,765-120,809,300	ATG5, LINC02518, 266 more genes
nsv3877239	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 94,202,605-109,878,834 , GRCh38.p12 chr6: 93,492,887-109,557,631	ATG5, RNA5SP211, 155 more genes
nsv4768376	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 98,949,950-114,533,905 , GRCh38.p12 chr6: 98,502,074-114,212,741	ATG5, LOC101927405, 211 more genes
nsv3874571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 97,384,446-110,247,755 , GRCh38.p12 chr6: 96,936,570-109,926,552	ATG5, NPM1P38, 130 more genes
nsv3919897	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 103,834,033-114,362,096 , GRCh37 chr6: 103,727,340-114,255,403 , GRCh38 chr6: 103,279,465-113,934,239	ATG5, HACE1, 174 more genes
nsv3913170	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 102,911,070-111,477,775 , GRCh38 chr6: 102,356,502-111,049,879 , GRCh37 chr6: 102,804,377-111,371,082	ATG5, RPS19P5, 121 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	ATG5, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	ATG5, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	ATG5, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ATG5, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	ATG5, RNU6-770P, 810 more genes
nsv4685989	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082	ATG5, RPL23AP50, 216 more genes
nsv3870479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 105,930,050-107,970,442 , GRCh38.p12 chr6: 105,482,175-107,649,238	ATG5, LINC02526, 29 more genes

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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 29

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Number of Variants: 20

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Supplemental Content

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