chrm4[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
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	CHRM4, FAUP4, 2031 more genes
nsv3922177	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 35,663,578-46,959,820 , GRCh37 chr11: 35,685,126-46,981,371 , NCBI36 chr11: 35,641,702-46,937,947	CHRM4, MIR3160-2, 122 more genes
nsv3913842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 39,200,802-49,157,287 , NCBI36 chr11: 39,157,378-49,113,863 , GRCh38 chr11: 39,179,252-49,135,735	CHRM4, MIR3160-1, 162 more genes
nsv3924778	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr11: 41,118,322-48,643,003 , GRCh37 chr11: 41,139,872-48,664,555 , NCBI36 chr11: 41,096,448-48,621,131	CHRM4, F2, 140 more genes
nsv6291196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr11: 40,117,145-46,920,718 , GRCh38.p12 chr11: 40,095,595-46,899,167	CHRM4, LINC02687, 86 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	CHRM4, 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	CHRM4, 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	CHRM4, 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	CHRM4, 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	CHRM4, TRR-TCT3-2, 494 more genes
nsv5380725	copy number variation	2	nstd102	human	Pathogenic, Uncertain significance	GRCh37 chr11: 45,827,353-47,804,770 , GRCh38.p12 chr11: 45,805,802-47,783,218	CHRM4, MIR4688, 58 more genes
nsv4729122	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr11: 45,995,260-46,536,343 , GRCh38.p12 chr11: 45,973,709-46,514,793	CHRM4, MDK, 13 more genes
nsv3914563	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr11: 42,705,681-49,113,863 , GRCh37 chr11: 42,749,105-49,157,287 , GRCh38 chr11: 42,727,555-49,135,735	CHRM4, ACP2, 143 more genes
nsv6313964	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,248,477-46,748,132 , GRCh38.p12 chr11: 46,226,926-46,726,582	CHRM4, ARHGAP1, 13 more genes
nsv4456633	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,302,171-46,783,079 , GRCh38.p12 chr11: 46,280,620-46,761,529	CHRM4, MIR5582, 15 more genes
nsv6309197	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,318,032-46,761,066 , GRCh38.p12 chr11: 46,296,481-46,739,516	CHRM4, MIR3160-2, 12 more genes
nsv4683154	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,387,807-46,766,127 , GRCh38.p12 chr11: 46,366,257-46,744,577	CHRM4, HARBI1, 12 more genes
nsv4729454	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,123,974-46,442,526 , GRCh38.p12 chr11: 46,102,423-46,420,976	CHRM4, MDK, 10 more genes
nsv3886462	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr11: 46,315,434-46,629,277 , GRCh38.p12 chr11: 46,293,883-46,607,727	CHRM4, HARBI1, 8 more genes

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chrm4[All Fields] AND 1[has_clinical] (20)
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