mcm6[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	MCM6, DAZAP2P1, 2991 more genes
nsv6290867	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 122,699,106-143,799,629 , GRCh38.p12 chr2: 121,941,530-143,042,060	MCM6, RNU6-675P, 300 more genes
nsv3876229	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 120,571,363-141,627,287 , GRCh38.p12 chr2: 119,813,787-140,869,718	MCM6, MIR9986, 320 more genes
nsv3897428	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 123,445,762-140,592,538 , NCBI36 chr2: 123,919,808-141,066,577 , GRCh37 chr2: 124,203,338-141,350,107	MCM6, ARHGAP42P2, 278 more genes
nsv3910856	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 134,449,789-141,806,260 , GRCh37.p13 chr2: 134,733,319-142,089,790 , GRCh38.p12 chr2: 133,975,748-141,332,221	MCM6, LOC105373643, 73 more genes
nsv4452826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 133,457,177-138,188,195 , GRCh38.p12 chr2: 132,699,604-137,430,625	MCM6, UBBP1, 42 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	MCM6, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	MCM6, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	MCM6, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	MCM6, MTND2P22, 3724 more genes
nsv6291353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036	MCM6, LINC01120, 490 more genes
nsv6314748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432	MCM6, MED15P9, 474 more genes
nsv5381338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882	MCM6, YY1P2, 156 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	MCM6, ACTG2, 1713 more genes
nsv3923963	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331	MCM6, NMTRQ-TTG9-1, 1944 more genes
nsv3876086	copy number variation	1	nstd102	human	drug response	GRCh37 chr2: 104,172,062-168,223,828 , GRCh38.p12 chr2: 103,555,604-167,367,318	MCM6, SLC4A10, 871 more genes
nsv7095856	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 135,809,878-136,875,630 , GRCh38.p12 chr2: 135,052,308-136,118,060	MCM6, G3BP1P1, 14 more genes
nsv7096367	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 136,545,894-136,875,630 , GRCh38.p12 chr2: 135,788,324-136,118,060	MCM6, DARS1-AS1, 5 more genes
nsv3924199	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr2: 130,861,065-242,751,149 , GRCh37.p13 chr2: 131,144,595-243,102,476 , GRCh38.p12 chr2: 130,387,022-242,160,331	MCM6, METAP1D, 1635 more genes
nsv4451808	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 135,712,129-137,818,795 , GRCh38.p12 chr2: 134,954,559-137,061,225	MCM6, MIR128-1, 22 more genes

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Number of Variants: 20

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