eif3m[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
nsv6634405	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 32,579,393-32,681,516 , GRCh38.p12 chr11: 32,557,847-32,659,970	EIF3M, CCDC73, 1 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	EIF3M, FAUP4, 2031 more genes
nsv3922664	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 22,550,115-38,199,159 , NCBI36 chr11: 22,528,237-38,177,285 , GRCh37 chr11: 22,571,661-38,220,709	EIF3M, CSTF3, 170 more genes
nsv3922794	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 20,101,020-34,485,543 , GRCh38 chr11: 20,079,474-34,463,996 , NCBI36 chr11: 20,057,596-34,442,119	EIF3M, LOC107984419, 150 more genes
nsv3898805	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 27,588,560-41,770,792 , GRCh38.p12 chr11: 27,567,013-41,749,242	EIF3M, LINC02707, 150 more genes
nsv4455873	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 22,079,154-35,597,645 , GRCh38.p12 chr11: 22,057,608-35,576,097	EIF3M, DNAJC24, 153 more genes
nsv3907223	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 24,469,451-37,524,085 , GRCh38.p12 chr11: 24,447,905-37,502,535	EIF3M, PIGCP1, 151 more genes
nsv3898238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 21,586,131-33,168,232 , GRCh38.p12 chr11: 21,564,585-33,146,686	EIF3M, RPS25P1, 114 more genes
nsv3906552	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 30,615,127-40,606,139 , GRCh38.p12 chr11: 30,593,580-40,584,589	EIF3M, MIR3973, 113 more genes
nsv3908389	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 25,771,208-35,614,978 , GRCh38.p12 chr11: 25,749,661-35,593,430	EIF3M, METTL15, 128 more genes
nsv3891217	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 25,196,998-34,196,484 , GRCh38.p12 chr11: 25,175,452-34,174,937	EIF3M, WT1-AS, 108 more genes
nsv3910889	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 26,368,962-35,252,976 , NCBI36 chr11: 26,347,085-35,231,099 , GRCh37 chr11: 26,390,509-35,274,523	EIF3M, WT1, 122 more genes
nsv6638023	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,372,721-38,259,316 , GRCh38.p12 chr11: 31,351,174-38,237,766	EIF3M, THEM7P, 92 more genes
nsv3900662	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 27,154,853-33,302,474 , GRCh38.p12 chr11: 27,133,306-33,280,928	EIF3M, LOC107984321, 81 more genes
nsv3899653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 31,210,842-35,436,121 , GRCh38.p12 chr11: 31,189,295-35,414,574	EIF3M, LOC101928385, 69 more genes
nsv3909118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 29,883,001-33,865,721 , GRCh38.p12 chr11: 29,861,454-33,844,175	EIF3M, LOC101928338, 56 more genes
nsv3904666	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 29,750,813-32,752,091 , GRCh38.p12 chr11: 29,729,266-32,730,545	EIF3M, LINC01616, 34 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	EIF3M, 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	EIF3M, 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	EIF3M, IGHMBP2, 2829 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 24

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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