dbVar for Gene (Select 594855) - 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
nsv5940399	copy number variation	1	nstd209	human		GRCh38 chr15: 74,823,435-74,833,001 , GRCh37.p13 chr15: 75,115,776-75,125,342	LMAN1L, CPLX3, 1 more genes
nsv5933606	copy number variation	1	nstd209	human		GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573	, STRA6, 229 more genes
nsv5864011	copy number variation	1	nstd209	human		GRCh38 chr15: 74,823,014-74,825,663 , GRCh37.p13 chr15: 75,115,355-75,118,004	LMAN1L, CPLX3
nsv5861145	copy number variation	1	nstd209	human		GRCh38 chr15: 74,828,365-74,829,704 , GRCh37.p13 chr15: 75,120,706-75,122,045	LOC105370897, CPLX3
nsv5849539	copy number variation	1	nstd209	human		GRCh38 chr15: 74,823,464-74,832,542 , GRCh37.p13 chr15: 75,115,805-75,124,883	LOC105370897, LMAN1L, 1 more genes
nsv5380758	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289	LOC105370794, HNRNPA1P45, 1173 more genes
nsv5009057	copy number variation	1	nstd200	human		GRCh38 chr15: 74,796,648-74,914,092 , GRCh37.p13 chr15: 75,088,989-75,206,433	CSK, SCAMP2, 7 more genes
nsv4992298	copy number variation	1	nstd200	human		GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519	, SNUPN, 215 more genes
nsv4729106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 74,398,162-76,054,094 , GRCh38.p12 chr15: 74,105,821-75,761,753	FAM219B, MIR4513, 62 more genes
nsv4675298	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 75,039,267-75,268,029 , GRCh38.p12 chr15: 74,746,926-74,975,688	SCAMP2, CSK, 11 more genes
nsv4455940	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183	TBC1D21, CPLX3, 72 more genes
nsv4455912	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,963,271-76,064,900 , GRCh38.p12 chr15: 72,670,930-75,772,559	MIR6881, ARID3B, 94 more genes
nsv4455687	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183	SCAMP2, LOC105376731, 74 more genes
nsv4243297	copy number variation	1	nstd166	human		GRCh37.p13 chr15: 75,118,988-75,168,017 , GRCh38.p12 chr15: 74,826,647-74,875,676	SCAMP2, ULK3, 3 more genes
nsv3922157	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189	GCHFR, SPPL2A, 1382 more genes
nsv3920789	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr15: 70,751,023-73,279,197 , GRCh37 chr15: 72,963,970-75,492,144 , GRCh38 chr15: 72,671,629-75,199,803	BBS4, CLK3, 67 more genes
nsv3920702	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 70,708,423-73,322,383 , GRCh37 chr15: 72,921,369-75,535,330 , GRCh38 chr15: 72,629,028-75,242,989	FKBP1AP2, EDC3, 73 more genes
nsv3920020	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr15: 72,685,231-75,727,625 , NCBI36 chr15: 70,764,625-73,807,021 , GRCh37 chr15: 72,977,572-76,019,966	STRA6, LOC105370891, 91 more genes
nsv3919468	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189	RNU6-18P, GOLGA8K, 1442 more genes
nsv3918770	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189	SNRPCP18, SNORD116-30, 1622 more genes

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Number of Variants: 20

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Has Clinical Interpretation

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Items: 1 to 20 of 154

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Number of Variants: 20

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