dbVar for Gene (Select 9440) - 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
nsv5971422	insertion	1	nstd209	human		GRCh38 chr11: 93,793,114-93,793,114 , GRCh37.p13 chr11: 93,526,280-93,526,280	MED17
nsv5909547	copy number variation	1	nstd209	human		GRCh38 chr11: 93,796,861-93,797,151 , GRCh37.p13 chr11: 93,530,027-93,530,317	MED17
nsv5698318	mobile element insertion	1	nstd211	human		GRCh38 chr11: 93,803,568-93,803,568 , GRCh37.p13 chr11: 93,536,734-93,536,734	MED17
nsv5672785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,529,566-93,535,148 , GRCh38.p12 chr11: 93,796,400-93,801,982	MED17
nsv5672639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,521,157-93,521,343 , GRCh38.p12 chr11: 93,787,991-93,788,177	MED17
nsv5497804	copy number variation	1	nstd206	human		GRCh38 chr11: 93,482,000-94,038,896 , GRCh37.p13 chr11: 93,215,166-93,772,062	SNORA1, HPRT1P3, 20 more genes
nsv5395487	mobile element insertion	1	nstd206	human		GRCh38 chr11: 93,803,568-93,803,619 , GRCh37.p13 chr11: 93,536,734-93,536,785	MED17
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	FAUP4, MMP7, 2031 more genes
nsv5330748	translocation	1	nstd200	human		GRCh37 chr11: 93,530,027-93,530,027 , GRCh37 chr11: 93,530,327-93,530,327 , GRCh38.p12 chr11: 93,796,861-93,796,861 , GRCh38.p12 chr11: 93,797,161-93,797,161	MED17
nsv4989175	copy number variation	1	nstd200	human		GRCh38 chr11: 93,501,300-93,857,533 , GRCh37.p13 chr11: 93,234,466-93,590,699	VSTM5, SNORA18, 17 more genes
nsv4971676	copy number variation	1	nstd200	human		GRCh38 chr11: 93,806,980-93,807,146 , GRCh37.p13 chr11: 93,540,146-93,540,312	MED17
nsv4971591	copy number variation	1	nstd200	human		GRCh38 chr11: 91,285,470-94,799,390 , GRCh37.p13 chr11: 91,018,638-94,532,556	, LOC105369429, 53 more genes
nsv4839969	copy number variation	1	nstd200	human		GRCh37 chr11: 91,018,638-94,532,556 , GRCh38.p12 chr11: 91,285,470-94,799,390	, MIR548L, 53 more genes
nsv4729052	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 92,615,227-93,592,229 , GRCh38.p12 chr11: 92,882,061-93,859,063	CEP295, RPL26P31, 26 more genes
nsv4683928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 93,517,670-93,545,240 , GRCh38.p12 chr11: 93,784,504-93,812,074	MED17
nsv4675146	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 93,297,444-94,041,273 , GRCh38.p12 chr11: 93,564,278-94,308,107	SCARNA9, SNORD5, 22 more genes
nsv4616044	copy number variation	1	nstd183	human		GRCh37 chr11: 93,319,098-93,964,452 , GRCh38.p12 chr11: 93,585,932-94,231,286	TAF1D, SNORD6, 21 more genes
nsv4451419	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 93,784,504-93,788,177 , GRCh37 chr11: 93,517,670-93,521,343	MED17
nsv4209247	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 93,530,032-93,530,572 , GRCh38.p12 chr11: 93,796,866-93,797,406	MED17
nsv4199608	copy number variation	1	nstd166	human		GRCh37.p13 chr11: 93,537,176-93,537,246 , GRCh38.p12 chr11: 93,804,010-93,804,080	MED17

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 139

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Number of Variants: 20

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