cnot11[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
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	CNOT11, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	CNOT11, CYP1B1-AS1, 1649 more genes
nsv3900303	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 101,234,070-105,679,157 , NCBI36 chr2: 101,216,964-105,662,046 , GRCh37 chr2: 101,850,532-106,295,614	CNOT11, LOC105373529, 68 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	CNOT11, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	CNOT11, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	CNOT11, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	CNOT11, MTND2P22, 3724 more genes
nsv3876227	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 96,353,030-114,045,463 , GRCh38.p12 chr2: 95,687,282-113,287,886	CNOT11, RNU4-8P, 346 more genes
nsv3902899	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 94,707,984-111,076,455 , GRCh38 chr2: 94,678,532-110,602,409 , GRCh37 chr2: 95,344,257-111,359,986	CNOT11, MTCO3P45, 325 more genes
nsv3877583	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 95,529,039-108,518,266 , GRCh38.p12 chr2: 94,863,294-107,901,810	CNOT11, RPL27AP4, 242 more genes
nsv3907326	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 97,672,522-110,211,318 , GRCh37 chr2: 98,288,985-110,968,895 , NCBI36 chr2: 97,655,417-110,326,184	CNOT11, RPL22P11, 212 more genes
nsv3906654	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 91,443,218-102,334,856 , NCBI36 chr2: 90,981,410-102,317,748 , GRCh37 chr2: 91,617,683-102,951,316	CNOT11, CHEK2P3, 197 more genes
nsv3899291	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 95,618,109-103,868,854 , GRCh38 chr2: 94,817,406-103,252,396 , NCBI36 chr2: 94,846,878-103,235,286	CNOT11, IGKV2OR2-10, 178 more genes
nsv3906499	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 100,361,404-108,455,759 , GRCh37 chr2: 100,994,972-109,089,327 , GRCh38 chr2: 100,378,510-108,472,871	CNOT11, LOC105373511, 132 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	CNOT11, ACTG2, 1713 more genes
nsv3895049	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr2: 98,394,668-101,619,801 , GRCh37 chr2: 99,028,236-102,253,369 , GRCh38 chr2: 98,411,773-101,636,907	CNOT11, INPP4A, 59 more genes
nsv6291008	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 101,699,537-106,383,710 , GRCh38.p12 chr2: 101,083,075-105,767,253	CNOT11, C2orf49, 71 more genes
nsv3879354	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 95,518,497-107,186,127 , GRCh38.p12 chr2: 94,852,752-106,569,671	CNOT11, CD8B2, 231 more genes
nsv3901000	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 100,461,179-106,481,797 , GRCh38 chr2: 100,478,285-106,498,909 , GRCh37 chr2: 101,094,747-107,115,365	CNOT11, LOC107985926, 102 more genes
nsv3894524	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 99,236,392-101,542,533 , GRCh38 chr2: 99,253,497-101,559,639 , GRCh37 chr2: 99,869,960-102,176,101	CNOT11, CREG2, 43 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 23

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Number of Variants: 20

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Supplemental Content

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Search details

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