casd1[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
nsv3881281	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 94,604,254-94,619,273 , GRCh37 chr7: 94,233,566-94,248,585	CASD1, SGCE
nsv6634607	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,232,052-94,238,873 , GRCh38 chr7: 94,602,740-94,609,561	CASD1, SGCE
nsv5673938	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,228,081-94,232,770 , GRCh38.p12 chr7: 94,598,769-94,603,458	CASD1, SGCE
nsv6312464	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,248,050-94,252,729 , GRCh38.p12 chr7: 94,618,738-94,623,417	CASD1, SGCE
nsv3886627	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 94,598,775-94,603,452 , GRCh37.p13 chr7: 94,228,087-94,232,764	CASD1, SGCE
nsv6312366	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,248,050-94,248,288 , GRCh38.p12 chr7: 94,618,738-94,618,976	CASD1, SGCE
nsv6312365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,232,582-94,232,784 , GRCh38.p12 chr7: 94,603,270-94,603,472	CASD1, SGCE
nsv3885946	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 94,628,182-94,628,379 , GRCh37 chr7: 94,257,494-94,257,691	CASD1, SGCE
nsv7097763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,252,617-94,252,729 , GRCh38.p12 chr7: 94,623,305-94,623,417	CASD1, SGCE
nsv6634640	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,252,695-94,252,791 , GRCh38 chr7: 94,623,383-94,623,479	CASD1, SGCE
nsv5673939	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,252,627-94,252,719 , GRCh38.p12 chr7: 94,623,315-94,623,407	CASD1, SGCE
nsv6312364	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 94,214,811-94,252,729 , GRCh38.p12 chr7: 94,585,499-94,623,417	CASD1, SGCE
nsv6312875	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,257,494-94,285,410 , GRCh38.p12 chr7: 94,628,182-94,656,098	CASD1, PEG10, 1 more genes
nsv997219	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr7: 94,214,536-94,285,521 , GRCh38.p12 chr7: 94,585,224-94,656,209	CASD1, SGCE, 1 more genes
nsv4681353	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 94,024,334-94,214,837 , GRCh38.p12 chr7: 94,395,022-94,585,525	CASD1, SGCE, 3 more genes
nsv3919361	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 94,373,041-94,510,143 , NCBI36 chr7: 93,840,289-93,977,391 , GRCh37 chr7: 94,002,353-94,139,455	CASD1, RNU6-1328P, 3 more genes
nsv1398406	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 94,156,496-94,285,902 , GRCh38.p12 chr7: 94,527,184-94,656,590	CASD1, PEG10, 2 more genes
nsv3872509	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 94,024,324-94,285,430 , GRCh38 chr7: 94,395,012-94,656,118	CASD1, COL1A2, 4 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	CASD1, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	CASD1, LOC107986817, 2014 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 39

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Number of Variants: 20

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Supplemental Content

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Search details

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