lyz[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4681833	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 69,742,189-69,746,999 , GRCh38.p12 chr12: 69,348,409-69,353,219	LYZ
nsv3892030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 69,608,090-89,629,345 , GRCh38.p12 chr12: 69,214,310-89,235,568	LYZ, LOC101928002, 197 more genes
nsv6112755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599	LYZ, LINC02421, 144 more genes
nsv7093395	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 64,609,458-70,352,103 , GRCh38.p12 chr12: 64,215,678-69,958,323	LYZ, TODL, 116 more genes
nsv3911433	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 64,125,223-69,706,384 , GRCh38 chr12: 65,445,176-71,026,337 , GRCh37 chr12: 65,838,956-71,420,117	LYZ, SLC35E3, 100 more genes
nsv4729265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 68,572,386-70,833,868 , GRCh38.p12 chr12: 68,178,606-70,440,088	LYZ, LINC02384, 47 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	LYZ, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	LYZ, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	LYZ, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	LYZ, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	LYZ, OR5BT1P, 2441 more genes
nsv3918556	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr12: 66,691,464-74,063,101 , GRCh37 chr12: 68,405,197-75,776,834 , GRCh38 chr12: 68,011,417-75,383,054	LYZ, CPM, 97 more genes
nsv6315114	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr12: 69,331,823-69,683,009 , GRCh37.p13 chr12: 69,725,603-70,076,789	LYZ, RN7SL804P, 11 more genes

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