snrnp25[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
nsv4682839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 97,132-193,701 , GRCh38.p12 chr16: 47,132-143,702	SNRNP25, MPG, 3 more genes
nsv6309958	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 97,132-163,851 , GRCh38.p12 chr16: 47,132-113,852	SNRNP25, NPRL3, 3 more genes
nsv3900235	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 97,133-109,978 , GRCh38.p12 chr16: 47,133-59,980	SNRNP25, POLR3K, 1 more genes
nsv6314956	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 96,766-137,939 , GRCh38.p12 chr16: 46,766-87,940	SNRNP25, NPRL3, 3 more genes
nsv3918555	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 96,766-130,409 , GRCh38 chr16: 46,766-80,410 , NCBI36 chr16: 36,766-70,409	SNRNP25, POLR3K, 2 more genes
nsv4456261	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr16: 85,880-111,198 , GRCh38.p12 chr16: 35,880-61,200	SNRNP25, POLR3K, 2 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	SNRNP25, 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	SNRNP25, 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	SNRNP25, 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	SNRNP25, 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	SNRNP25, 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	SNRNP25, 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	SNRNP25, 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	SNRNP25, CACNA1H, 100 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	SNRNP25, CIAO3, 95 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	SNRNP25, PIGQ, 92 more genes
nsv3897068	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,498,731 , GRCh38.p12 chr16: 35,880-1,448,730	SNRNP25, TPSG1, 91 more genes
nsv6314105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,468,828 , GRCh38.p12 chr16: 35,880-1,418,827	SNRNP25, HBA2, 87 more genes
nsv4455728	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,468,459 , GRCh38.p12 chr16: 35,880-1,418,458	SNRNP25, GNG13, 87 more genes
nsv6637972	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185	SNRNP25, MPG, 78 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 62

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Number of Variants: 20

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