nme4[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
nsv3894522	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 449,695-474,204 , GRCh38.p12 chr16: 399,695-424,204 , GRCh38.p12 chr16\|NT_187610.1: 1-23,350	NME4, DECR2, 1 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, 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	NME4, TPSG1, 91 more genes
nsv7094663	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266	NME4, TPSP2, 83 more genes
nsv3920650	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 95,427-1,489,895 , GRCh37 chr16: 155,427-1,549,894 , GRCh38 chr16: 105,429-1,499,893	NME4, LOC101929440, 89 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	NME4, 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	NME4, 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	NME4, MPG, 78 more genes
nsv3911195	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr16: 49,978-1,211,652 , GRCh38 chr16: 59,980-1,221,651 , GRCh37 chr16: 109,978-1,271,651	NME4, LOC107984906, 69 more genes
nsv4676068	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 85,880-1,166,355 , GRCh38.p12 chr16: 35,880-1,116,355	NME4, LINC00235, 69 more genes
nsv3912118	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr16: 46,766-882,211 , GRCh37 chr16: 96,766-932,211 , NCBI36 chr16: 36,766-872,212	NME4, PIGQ, 60 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 68

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Number of Variants: 20

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