dbVar for Gene (Select 6011) - 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
nsv7148164	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr13: 106,425,676-114,326,445 , GRCh37.p13 chr13: 107,078,024-115,085,141	TUBGCP3, LINC01043, 132 more genes
nsv7144611	copy number variation	1	nstd232	human		GRCh37.p13 chr13: 114,440,309-114,440,445 , GRCh38.p12 chr13: 113,737,336-113,737,472 , GRCh38.p12 chr13\|NT_187596.1: 10,447-10,583	GRK1
nsv7066153	inversion	1	nstd229	human		GRCh38 chr13: 113,377,803-114,332,425 , GRCh37.p13 chr13: 114,032,118-115,085,141	TMCO3, GRK1, 26 more genes
nsv6957370	copy number variation	1	nstd229	human		GRCh38 chr13: 113,732,685-113,740,880 , GRCh37.p13 chr13: 114,435,658-114,443,853	LOC105377805, GRK1
nsv6954422	copy number variation	1	nstd229	human		GRCh38 chr13: 113,733,511-113,733,794 , GRCh37.p13 chr13: 114,436,484-114,436,767	GRK1
nsv6952191	copy number variation	1	nstd229	human		GRCh38 chr13: 113,653,196-113,653,322 , GRCh37.p13 chr13: 114,307,511-114,307,637	GRK1, ATP4B
nsv6949016	copy number variation	1	nstd229	human		GRCh38 chr13: 113,660,855-113,668,408 , GRCh37.p13 chr13: 114,315,170-114,322,723	GRK1
nsv6947535	copy number variation	1	nstd229	human		GRCh38 chr13: 113,725,969-113,732,129 , GRCh37.p13 chr13: 114,428,942-114,435,102	GRK1
nsv6943585	copy number variation	1	nstd229	human		GRCh38 chr13: 113,735,340-113,817,371 , GRCh37.p13 chr13: 114,438,313-114,520,344	GRK1, TMEM255B, 3 more genes
nsv6942847	copy number variation	1	nstd229	human		GRCh38 chr13: 113,098,406-113,791,902 , GRCh37.p13 chr13: 113,752,720-114,494,875	MIR8075, ATP4B, 22 more genes
nsv6939965	copy number variation	1	nstd229	human		GRCh38 chr13: 113,656,337-113,662,743 , GRCh37.p13 chr13: 114,310,652-114,317,058	ATP4B, GRK1
nsv6939661	copy number variation	1	nstd229	human		GRCh38 chr13: 113,647,669-113,647,747 , GRCh37.p13 chr13: 114,301,984-114,302,062	ATP4B, GRK1
nsv6939602	copy number variation	1	nstd229	human		GRCh38 chr13: 113,732,200-113,747,054 , GRCh37.p13 chr13: 114,435,173-114,450,027	LOC105377805, LINC00552, 1 more genes
nsv6939564	copy number variation	1	nstd229	human		GRCh38 chr13: 113,666,150-113,666,193 , GRCh37.p13 chr13: 114,320,465-114,320,508	GRK1
nsv6939406	copy number variation	1	nstd229	human		GRCh38 chr13: 113,617,461-113,789,008 , GRCh37.p13 chr13: 114,271,776-114,491,981	TFDP1, LINC00552, 4 more genes
nsv6938825	copy number variation	1	nstd229	human		GRCh38 chr13: 113,648,501-113,656,800 , GRCh37.p13 chr13: 114,302,816-114,311,115	ATP4B, GRK1
nsv6938484	copy number variation	1	nstd229	human		GRCh38 chr13: 113,562,955-114,319,153 , GRCh37.p13 chr13: 114,217,270-115,084,628	CDC16, TMEM255B, 21 more genes
nsv6638047	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 75,268,539-115,107,733 , GRCh38.p12 chr13: 74,694,402-114,342,258	CUL4A, LOC105370373, 488 more genes
nsv6637525	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr13: 114,318,476-114,549,197 , GRCh38.p12 chr13: 113,664,161-113,846,224	TMEM255B, LOC105377805, 4 more genes
nsv6637400	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr13: 97,142,120-115,107,733 , GRCh38.p12 chr13: 96,489,866-114,342,258	LOC107984609, LINC00354, 265 more genes

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 467

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Number of Variants: 20

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