rs1[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
nsv7098246	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,674,753-18,675,805 , GRCh38.p12 chrX: 18,656,633-18,657,685	RS1
nsv5673982	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,674,761-18,675,795 , GRCh38.p12 chrX: 18,656,641-18,657,675	RS1
nsv7098011	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,674,753-18,674,898 , GRCh38.p12 chrX: 18,656,633-18,656,778	RS1
nsv7098362	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chrX: 18,690,117-18,690,188 , GRCh38.p12 chrX: 18,671,997-18,672,068	RS1
nsv5674086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,675,740-18,675,805 , GRCh38.p12 chrX: 18,657,620-18,657,685	RS1
nsv5674193	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,690,137-18,690,188 , GRCh38.p12 chrX: 18,672,017-18,672,068	RS1
nsv5381710	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 18,675,494-18,676,498 , GRCh38 chrX: 18,657,374-18,658,378	RS1
nsv5673909	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,582,587-18,690,188 , GRCh38.p12 chrX: 18,564,467-18,672,068	RS1, CDKL5
nsv3876202	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chrX: 18,575,354-18,653,629 , GRCh37 chrX: 18,593,474-18,671,749	RS1, CDKL5
nsv3881314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,643,248-18,671,749 , GRCh38 chrX: 18,625,128-18,653,629	RS1, CDKL5
nsv3906981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,662,177-18,690,178 , GRCh38 chrX: 18,644,057-18,672,058 , NCBI36 chrX: 18,572,098-18,600,099	RS1, CDKL5
nsv7098608	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,662,530-18,690,188 , GRCh38.p12 chrX: 18,644,410-18,672,068	RS1, CDKL5
nsv5673910	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,662,550-18,690,188 , GRCh38.p12 chrX: 18,644,430-18,672,068	RS1, CDKL5
nsv3887415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,646,491-18,671,749 , GRCh38 chrX: 18,628,371-18,653,629	RS1, CDKL5
nsv7098360	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,663,320-18,665,330 , GRCh38.p12 chrX: 18,645,200-18,647,210	RS1, CDKL5
nsv7098609	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chrX: 18,665,301-18,665,462 , GRCh38.p12 chrX: 18,647,181-18,647,342	RS1, CDKL5
nsv997098	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chrX: 18,657,808-18,690,223 , GRCh38.p12 chrX: 18,639,688-18,672,103	RS1, CDKL5
nsv3907660	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chrX: 18,498,514-18,579,094 , GRCh37 chrX: 18,588,593-18,669,173 , GRCh38 chrX: 18,570,473-18,651,053	RS1, CDKL5
nsv6314997	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chrX: 18,662,662-18,662,759 , GRCh38 chrX: 18,644,542-18,644,639	RS1, CDKL5
nsv3880503	copy number variation	1	nstd102	human	Benign	GRCh37 chrX: 18,662,484-18,662,736 , GRCh38.p12 chrX: 18,644,364-18,644,616	RS1, CDKL5

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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 319

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Number of Variants: 20

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