epha7[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
nsv3873760	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 93,954,830-94,119,909 , GRCh38.p12 chr6: 93,245,112-93,410,191	EPHA7
nsv4457204	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 93,944,739-94,086,819 , GRCh38.p12 chr6: 93,235,021-93,377,101	EPHA7
nsv3911641	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 94,129,521-94,322,628 , GRCh37.p13 chr6: 94,072,800-94,265,907 , GRCh38.p12 chr6: 93,363,082-93,556,189	EPHA7, LOC105377899
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	EPHA7, 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	EPHA7, RN7SL509P, 311 more genes
nsv3923528	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 84,604,741-99,376,910 , GRCh38 chr6: 83,838,303-98,822,313 , GRCh37 chr6: 84,548,022-99,270,189	EPHA7, RNU4-72P, 157 more genes
nsv3879439	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 92,576,950-104,658,245 , GRCh38.p12 chr6: 91,867,232-104,210,370	EPHA7, FBXL4, 75 more genes
nsv3914309	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 82,569,098-93,753,476 , NCBI36 chr6: 83,335,534-94,519,915 , GRCh37 chr6: 83,278,815-94,463,194	EPHA7, ME1, 136 more genes
nsv3922912	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 90,687,494-93,806,515 , NCBI36 chr6: 91,453,934-94,572,954 , GRCh37 chr6: 91,397,213-94,516,233	EPHA7, LOC107986625, 18 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	EPHA7, 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	EPHA7, 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	EPHA7, 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	EPHA7, 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	EPHA7, RNU6-770P, 810 more genes
nsv6313857	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492	EPHA7, LOC101928570, 288 more genes
nsv3872975	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 81,261,418-97,796,269 , GRCh38.p12 chr6: 80,551,701-97,348,393	EPHA7, ME1, 178 more genes
nsv3889895	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr6: 89,941,373-95,634,177 , GRCh38.p12 chr6: 89,231,654-94,924,459	EPHA7, RN7SKP110, 46 more genes
nsv4675109	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 93,360,835-95,090,661 , GRCh38.p12 chr6: 92,651,117-94,380,943	EPHA7, TSG1, 5 more genes
nsv6634392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297	EPHA7, MTHFD2P2, 212 more genes
nsv3915765	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 91,425,377-94,604,519 , GRCh37.p13 chr6: 91,368,656-94,547,798 , GRCh38.p12 chr6: 90,658,937-93,838,080	EPHA7, LOC105377894, 18 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 22

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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