clcn7[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
nsv7094556	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,496,632-1,524,975 , GRCh38.p12 chr16: 1,446,631-1,474,974	CLCN7
nsv6309650	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,507,235-1,524,975 , GRCh38.p12 chr16: 1,457,234-1,474,974	CLCN7
nsv6314271	insertion	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,507,329-1,507,329 , GRCh38 chr16: 1,457,328-1,457,328	CLCN7
nsv6309844	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,515,346-1,521,214 , GRCh38.p12 chr16: 1,465,345-1,471,213	CLCN7
nsv6309833	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr16: 1,457,329-1,457,578 , GRCh37 chr16: 1,507,330-1,507,579	CLCN7
nsv6309990	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,515,248-1,515,359 , GRCh38.p12 chr16: 1,465,247-1,465,358	CLCN7
nsv7093350	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,507,330-1,507,379 , GRCh38 chr16: 1,457,329-1,457,378	CLCN7
nsv7094811	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 1,496,632-1,561,171 , GRCh38.p12 chr16: 1,446,631-1,511,170	CLCN7, IFT140, 3 more genes
nsv4455594	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-2,053,328 , GRCh38.p12 chr16: 35,880-2,003,327	CLCN7, JPT2, 128 more genes
nsv3919589	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 36,766-1,987,584 , GRCh37 chr16: 96,766-2,047,583 , GRCh38 chr16: 46,766-1,997,582	CLCN7, C1QTNF8, 127 more genes
nsv3914731	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 46,722-1,867,327 , NCBI36 chr16: 36,722-1,857,329 , GRCh37 chr16: 96,722-1,917,328	CLCN7, TPSP2, 110 more genes
nsv3897602	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,875,694 , GRCh38.p12 chr16: 35,880-1,825,693	CLCN7, CHTF18, 110 more genes
nsv3919625	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 23,141-1,773,349 , NCBI36 chr16: 13,141-1,763,351 , GRCh37 chr16: 73,141-1,823,350	CLCN7, RHOT2, 106 more genes
nsv3916129	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 13,141-1,702,525 , GRCh38 chr16: 23,141-1,712,523 , GRCh37 chr16: 73,141-1,762,524	CLCN7, C4orf46P1, 102 more genes
nsv3906615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 88,165-1,715,454 , GRCh38.p12 chr16: 38,165-1,665,453	CLCN7, LOC105371046, 97 more genes
nsv3890088	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 61,451-1,593,645 , GRCh38.p12 chr16: 11,451-1,543,644	CLCN7, CACNA1H, 100 more genes
nsv4683390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004	CLCN7, MRPS34, 102 more genes
nsv3920214	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 46,766-1,544,014 , NCBI36 chr16: 36,766-1,534,016 , GRCh37 chr16: 96,766-1,594,015	CLCN7, CIAO3, 95 more genes
nsv4449893	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 624,055-2,115,656 , GRCh38.p12 chr16: 574,055-2,065,655	CLCN7, LMF1-AS1, 99 more genes
nsv3894432	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 72,769-1,511,716 , GRCh38.p12 chr16: 22,769-1,461,715	CLCN7, PIGQ, 92 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 67

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Number of Variants: 20

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