idua[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
nsv6311734	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 994,390-998,355 , GRCh38.p12 chr4: 1,000,602-1,004,567	IDUA
nsv5673571	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 996,510-998,355 , GRCh38.p12 chr4: 1,002,722-1,004,567	IDUA
nsv7136956	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 996,520-998,294 , GRCh37 chr4: 990,308-992,082	IDUA
nsv4685607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 996,510-998,191 , GRCh38 chr4: 1,002,722-1,004,403	IDUA
nsv5980381	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr4: 995,358-995,359 , GRCh38 chr4: 1,001,570-1,001,571	IDUA
nsv6311733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 980,775-981,747 , GRCh38.p12 chr4: 986,987-987,959	IDUA, SLC26A1
nsv7097010	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 980,775-981,040 , GRCh38.p12 chr4: 986,987-987,252	IDUA, SLC26A1
nsv3872798	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 981,734-984,948 , GRCh38.p12 chr4: 987,946-991,160	IDUA, SLC26A1
nsv7096869	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 980,871-985,491 , GRCh38.p12 chr4: 987,083-991,703	IDUA, SLC26A1
nsv7097011	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 980,871-981,050 , GRCh38.p12 chr4: 987,083-987,262	IDUA, SLC26A1
nsv3880412	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 954,449-985,418 , GRCh38.p12 chr4: 960,661-991,630	IDUA, SLC26A1, 1 more genes
nsv3873278	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 954,449-985,076 , GRCh38.p12 chr4: 960,661-991,288	IDUA, SLC26A1, 1 more genes
nsv3871570	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 947,035-1,019,312 , GRCh38.p12 chr4: 953,247-1,025,524	IDUA, SLC26A1, 3 more genes
nsv3876082	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 947,024-1,019,101 , GRCh38.p12 chr4: 953,236-1,025,313	IDUA, FGFRL1, 3 more genes
nsv3882732	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 947,035-1,019,101 , GRCh38.p12 chr4: 953,247-1,025,313	IDUA, SLC26A1, 3 more genes
nsv3922676	copy number variation	1	nstd102	human	Benign/Likely benign	NCBI36 chr4: 942,406-1,010,417 , GRCh38 chr4: 958,618-1,026,629 , GRCh37 chr4: 952,406-1,020,417	IDUA, FGFRL1, 3 more genes
nsv3918564	copy number variation	1	nstd102	human	Benign	NCBI36 chr4: 942,465-1,010,417 , GRCh37 chr4: 952,465-1,020,417 , GRCh38 chr4: 958,677-1,026,629	IDUA, DGKQ, 3 more genes
nsv3889162	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 954,422-1,019,312 , GRCh38.p12 chr4: 960,634-1,025,524	IDUA, SLC26A1, 2 more genes
nsv3875424	copy number variation	1	nstd102	human	Benign	GRCh37 chr4: 954,449-1,019,312 , GRCh38.p12 chr4: 960,661-1,025,524	IDUA, FGFRL1, 2 more genes
nsv3911405	copy number variation	1	nstd102	human	Benign	GRCh38 chr4: 975,137-1,026,688 , GRCh37 chr4: 968,925-1,020,476 , NCBI36 chr4: 958,925-1,010,476	IDUA, FGFRL1, 1 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 171

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Number of Variants: 20

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