chd2[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
nsv3919031	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 91,307,893-91,375,475 , GRCh37 chr15: 93,506,889-93,574,471 , GRCh38 chr15: 92,963,659-93,031,241	CHD2
nsv4681731	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,510,535-93,555,694 , GRCh38.p12 chr15: 92,967,305-93,012,464	CHD2
nsv7094644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,485,032-93,515,667 , GRCh38.p12 chr15: 92,941,802-92,972,437	CHD2
nsv3888171	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 92,996,937-93,014,929 , GRCh37 chr15: 93,540,167-93,558,159	CHD2
nsv4682284	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,482,788-93,487,765 , GRCh38.p12 chr15: 92,939,558-92,944,535	CHD2
nsv5672831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,514,985-93,518,190 , GRCh38.p12 chr15: 92,971,755-92,974,960	CHD2
nsv6309644	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,521,444-93,522,533 , GRCh38.p12 chr15: 92,978,214-92,979,303	CHD2
nsv6309814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,489,031-93,489,466 , GRCh38.p12 chr15: 92,945,801-92,946,236	CHD2
nsv7094747	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,528,708-93,528,923 , GRCh38.p12 chr15: 92,985,478-92,985,693	CHD2
nsv4682719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,472,240-93,472,341 , GRCh38.p12 chr15: 92,929,010-92,929,111	CHD2
nsv4682678	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,444,448-93,444,549 , GRCh38.p12 chr15: 92,901,218-92,901,319	CHD2
nsv7093309	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,498,735-93,498,788 , GRCh38 chr15: 92,955,505-92,955,558	CHD2
nsv5674324	delins	1	nstd102	human	Pathogenic	GRCh37 chr15: 93,540,229-93,540,235 , GRCh38 chr15: 92,996,999-92,997,005	CHD2
nsv7094549	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr15: 93,547,827-93,558,159 , GRCh38.p12 chr15: 93,004,597-93,014,929	CHD2
nsv3902195	copy number variation	1	nstd102	human	Benign	GRCh37 chr21: 41,521,231-41,521,681 , GRCh38.p12 chr21: 40,149,304-40,149,754	DSCAM
nsv6634539	copy number variation	1	nstd102	human	Benign	GRCh38 chr15: 92,972,558-92,972,870 , GRCh37 chr15: 93,515,788-93,516,100	CHD2
nsv6309815	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 93,510,535-93,567,935 , GRCh38.p12 chr15: 92,967,305-93,024,705	CHD2
nsv3918709	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 91,321,456-91,374,888 , GRCh37.p13 chr15: 93,520,452-93,573,884 , GRCh38.p12 chr15: 92,977,222-93,030,654	CHD2
nsv6309981	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 93,522,345-93,567,935 , GRCh38.p12 chr15: 92,979,115-93,024,705	CHD2
nsv3873548	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 93,496,567-93,528,923 , GRCh38 chr15: 92,953,337-92,985,693	CHD2

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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 153

Page of 8

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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