dbVar for Gene (Select 284276) - 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
nsv7148195	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 63,476,940-77,960,815 , GRCh38.p12 chr18: 65,809,704-80,202,932	LOC105372202, LINC01896, 149 more genes
nsv7137214	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 66,057,406-78,014,123 , GRCh38.p12 chr18: 68,390,169-80,256,240	LOC105372228, MIR548AV, 132 more genes
nsv7137137	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 71,740,696-78,005,231 , GRCh38.p12 chr18: 74,073,461-80,247,348	LOC339298, LOC105372201, 84 more genes
nsv7099035	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 66,434,850-78,075,000 , GRCh38.p12 chr18: 68,767,613-80,259,271	LOC107985151, CD226, 129 more genes
nsv7016779	copy number variation	1	nstd229	human		GRCh38 chr18: 76,559,379-76,559,440 , GRCh37.p13 chr18: 74,271,336-74,271,397	LINC00908
nsv7015592	copy number variation	1	nstd229	human		GRCh38 chr18: 76,497,101-76,900,200 , GRCh37.p13 chr18: 74,209,058-74,612,156	LOC107985151, RNU6-346P, 14 more genes
nsv7014752	copy number variation	1	nstd229	human		GRCh38 chr18: 76,533,201-76,566,900 , GRCh37.p13 chr18: 74,245,158-74,278,857	LINC00908
nsv7006547	copy number variation	1	nstd229	human		GRCh38 chr18: 76,531,078-76,531,135 , GRCh37.p13 chr18: 74,243,035-74,243,092	LINC00908
nsv7004521	copy number variation	1	nstd229	human		GRCh38 chr18: 76,490,801-76,573,800 , GRCh37.p13 chr18: 74,202,757-74,285,757	ZNF516, LINC00908, 2 more genes
nsv7002259	copy number variation	1	nstd229	human		GRCh38 chr18: 76,548,196-76,560,509 , GRCh37.p13 chr18: 74,260,153-74,272,466	LINC00908
nsv6998222	copy number variation	1	nstd229	human		GRCh38 chr18: 76,545,401-76,550,000 , GRCh37.p13 chr18: 74,257,358-74,261,957	LINC00908
nsv6638045	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 66,530,142-78,014,123 , GRCh38.p12 chr18: 68,862,905-80,256,240	LOC105372211, LOC105372188, 128 more genes
nsv6638004	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 61,520,071-78,014,123 , GRCh38.p12 chr18: 63,852,837-80,256,240	LOC107985151, CD226, 165 more genes
nsv6637467	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 53,624,405-78,014,123 , GRCh38.p12 chr18: 55,957,174-80,256,240	RPL9P31, LOC100422317, 277 more genes
nsv6637395	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr18: 73,711,236-74,360,445 , GRCh38.p12 chr18: 75,999,281-76,648,488	LOC105372204, LOC339298, 12 more genes
nsv6634444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 72,669,936-77,889,946 , GRCh38.p12 chr18: 74,957,980-80,132,063	LOC105372212, GALR1, 71 more genes
nsv6532224	copy number variation	1	nstd223	human		GRCh38 chr18: 76,533,108-76,533,575 , GRCh37.p13 chr18: 74,245,065-74,245,532	LINC00908
nsv6527466	copy number variation	1	nstd223	human		GRCh38 chr18: 76,540,135-76,542,100 , GRCh37.p13 chr18: 74,252,092-74,254,057	LINC00908
nsv6527278	copy number variation	1	nstd223	human		GRCh38 chr18: 76,533,395-76,541,892 , GRCh37.p13 chr18: 74,245,352-74,253,849	LINC00908
nsv6524194	copy number variation	1	nstd223	human		GRCh38 chr18: 76,538,192-76,540,456 , GRCh37.p13 chr18: 74,250,149-74,252,413	LINC00908

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Number of Variants: 20

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Items: 1 to 20 of 444

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Number of Variants: 20

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