bcl3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3891669	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 43,013,365-47,241,534 , GRCh38.p12 chr19: 42,509,213-46,738,277	BCL3, MIR320E, 189 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	BCL3, 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	BCL3, 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	BCL3, LENG8, 2408 more genes
nsv4457372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575	BCL3, ZNF461, 735 more genes
nsv4676357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308	BCL3, MIR4324, 485 more genes
nsv3890841	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 44,300,416-45,639,540 , GRCh38.p12 chr19: 43,796,264-45,136,282	BCL3, ZNF225, 57 more genes
nsv6314081	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 45,074,342-46,133,841 , GRCh38.p12 chr19: 44,571,096-45,630,583	BCL3, EXOC3L2, 50 more genes
nsv4436634	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 43,997,366-44,819,487 , GRCh37 chr19: 44,501,518-45,322,744	BCL3, BCAM, 34 more genes

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