eci2[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
nsv3921817	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,862,874-16,698,019 , GRCh38 chr6: 2,862,640-16,697,788 , NCBI36 chr6: 2,807,873-16,805,998	ECI2, RN7SKP293, 230 more genes
nsv3911792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 101,974-13,964,135 , GRCh38 chr6: 156,974-13,855,925 , GRCh37 chr6: 156,974-13,856,156	ECI2, SIRT5, 228 more genes
nsv3873362	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 204,009-11,608,587 , GRCh38.p12 chr6: 204,009-11,608,354	ECI2, LOC100506207, 193 more genes
nsv3914068	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 4,014,025-13,376,010 , GRCh38 chr6: 4,068,792-13,267,799 , GRCh37 chr6: 4,069,026-13,268,031	ECI2, SSR1, 145 more genes
nsv3923249	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267	ECI2, LOC100506207, 148 more genes
nsv3916436	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-7,122,992 , NCBI36 chr6: 101,974-7,067,991 , GRCh38 chr6: 156,974-7,122,759	ECI2, LINC01011, 119 more genes
nsv3883703	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 156,974-6,417,749 , GRCh38.p12 chr6: 156,974-6,417,516	ECI2, LOC107986514, 108 more genes
nsv3875400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 204,009-6,447,311 , GRCh38.p12 chr6: 204,009-6,447,078	ECI2, FAM217A, 107 more genes
nsv3914400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 97,634-6,235,036 , GRCh38 chr6: 152,634-6,289,804 , GRCh37 chr6: 152,634-6,290,037	ECI2, LOC105374898, 106 more genes
nsv3922576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 164,633-6,284,470 , GRCh38 chr6: 164,633-6,284,237 , NCBI36 chr6: 109,633-6,229,469	ECI2, GLRX3P2, 106 more genes
nsv3914814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,083-6,063,033 , GRCh38 chr6: 163,083-6,062,800 , NCBI36 chr6: 108,083-6,008,032	ECI2, LINC02521, 103 more genes
nsv3912779	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 163,083-5,875,635 , GRCh38 chr6: 163,083-5,875,402 , NCBI36 chr6: 108,083-5,820,634	ECI2, CRIPTOP4, 98 more genes
nsv3920236	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 164,633-5,823,834 , GRCh38 chr6: 164,633-5,823,601 , NCBI36 chr6: 109,633-5,768,833	ECI2, TUBB2A, 98 more genes
nsv3915132	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,634-5,315,912 , GRCh38 chr6: 152,634-5,315,679 , NCBI36 chr6: 97,634-5,260,911	ECI2, LOC101927888, 94 more genes
nsv3910975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 107,682-4,979,015 , NCBI36 chr6: 52,682-4,924,014 , GRCh38 chr6: 107,682-4,978,781	ECI2, RNA5SP201, 90 more genes
nsv3916403	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-4,907,692 , GRCh37 chr6: 156,974-4,907,926 , NCBI36 chr6: 101,974-4,852,925	ECI2, MIR6720, 86 more genes
nsv3877391	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 2,109,893-5,962,832 , GRCh38.p12 chr6: 2,109,659-5,962,599	ECI2, LOC107986516, 76 more genes
nsv3882883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 383,951-4,183,288 , GRCh38.p12 chr6: 383,951-4,183,054	ECI2, TUBB2BP1, 69 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	ECI2, 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	ECI2, RNU6-411P, 2910 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 44

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Number of Variants: 20

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Search details

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