dbVar for Gene (Select 400658) - 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
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
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
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
nsv6519061	copy number variation	1	nstd223	human		GRCh38 chr18: 76,496,886-76,497,278 , GRCh37.p13 chr18: 74,208,843-74,209,235	ZNF516-DT
nsv6315531	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 61,289,055-78,014,123 , GRCh38.p12 chr18: 63,621,821-80,256,240	RN7SL795P, ZNF407, 169 more genes
nsv6315530	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271	LOC105372145, LOC105372016, 947 more genes
nsv6315301	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 61,490,305-80,247,612 , GRCh37.p13 chr18: 59,157,538-78,005,495	RN7SL705P, LOC105372166, 196 more genes
nsv6314804	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr18: 69,541,066-80,373,285 , GRCh37.p13 chr18: 67,208,302-78,017,154	LIVAR, DOK6, 122 more genes
nsv6314216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 52,675,201-78,014,123 , GRCh38.p12 chr18: 55,007,970-80,256,240	RNA5SP461, CYB5A, 290 more genes
nsv6314188	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 53,309,113-78,014,123 , GRCh38.p12 chr18: 55,641,882-80,256,240	ZNF236-DT, SERPINB2, 282 more genes
nsv6314140	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 70,333,866-78,014,123 , GRCh38.p12 chr18: 72,666,631-80,256,240	CTDP1-DT, DIPK1C, 93 more genes
nsv6314111	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr18: 58,305,972-78,014,123 , GRCh38.p12 chr18: 60,638,739-80,256,240	LOC101927897, CTDP1, 202 more genes

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dbVar

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Organism

Variant Type

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 396

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Number of Variants: 20

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