fbxl12[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 10

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,846,119-11,338,677 , GRCh38 chr19: 9,735,443-11,228,001 , NCBI36 chr19: 9,707,119-11,199,677	FBXL12, PPAN, 68 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	FBXL12, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	FBXL12, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	FBXL12, LENG8, 2408 more genes
nsv3898900	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 9,678,768-14,853,426 , GRCh38.p12 chr19: 9,568,092-14,742,614	FBXL12, DCAF15, 253 more genes
nsv3920616	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227	FBXL12, ACP5, 236 more genes
nsv3888397	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059	FBXL12, ELAVL1, 80 more genes
nsv1398241	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 8,661,944-10,104,083 , GRCh38.p12 chr19: 8,597,060-9,993,407	FBXL12, MUC16, 58 more genes
nsv4729799	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622	FBXL12, ZNF426-DT, 61 more genes
nsv4436244	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054	FBXL12, PIN1, 51 more genes

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