gnptg[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
nsv4453599	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 1,401,957-1,413,102 , GRCh38 chr16: 1,351,956-1,363,101	GNPTG, UNKL, 1 more genes
nsv3907357	copy number variation	1	nstd102	human	Benign	GRCh37 chr16: 1,414,498-1,423,967 , GRCh38.p12 chr16: 1,364,497-1,373,966	GNPTG, TJP1P1, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, 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	GNPTG, GNG13, 87 more genes
nsv7098880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 811,896-2,130,379 , GRCh38.p12 chr16: 761,896-2,080,378	GNPTG, TPSP1, 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 61

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Number of Variants: 20

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