med19[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5672633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 57,471,510-57,564,464 , GRCh38.p12 chr11: 57,704,038-57,796,992	MED19, CTNND1, 5 more genes
nsv5380796	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397	MED19, FAUP4, 2031 more genes
nsv3893233	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576	MED19, LOC105376598, 2842 more genes
nsv3900144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169	MED19, RTN3, 2833 more genes
nsv3908873	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576	MED19, IGHMBP2, 2829 more genes
nsv6315537	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576	MED19, PYGM, 2125 more genes
nsv6315474	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 43,607,886-61,466,671 , GRCh38.p12 chr11: 43,586,336-61,699,199	MED19, TRR-TCT3-2, 494 more genes
nsv3911150	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 55,086,995-58,766,250 , NCBI36 chr11: 54,843,571-58,522,826 , GRCh38 chr11: 55,319,519-58,998,777	MED19, OR5BD1P, 197 more genes
nsv3899876	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 57,147,016-57,667,222 , GRCh38.p12 chr11: 57,379,543-57,899,750	MED19, PRG3, 24 more genes
nsv3894955	copy number variation	1	nstd102	human	Benign	GRCh37 chr11: 57,306,011-57,669,349 , GRCh38.p12 chr11: 57,538,538-57,901,877	MED19, SELENOH, 16 more genes
nsv3904152	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 49,313,405-59,008,426 , GRCh38.p12 chr11: 49,291,853-59,240,953	MED19, FAM111B, 250 more genes
nsv4453292	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 55,033,164-57,518,726 , GRCh38.p12 chr11: 55,265,688-57,751,254	MED19, OR8J3, 150 more genes
nsv6291401	copy number variation	1	nstd102	human	not provided	GRCh37 chr11: 57,112,299-57,871,866 , GRCh38.p12 chr11: 57,344,825-58,104,394	MED19, RN7SL605P, 35 more genes
nsv3918477	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr11: 57,372,226-57,936,167 , NCBI36 chr11: 56,896,275-57,460,215 , GRCh37 chr11: 57,139,699-57,703,639	MED19, TMX2-CTNND1, 26 more genes

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