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

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3901852	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 91,496,137-91,749,981 , GRCh38.p12 chr12: 91,102,360-91,356,204	DCN, LUM, 2 more genes
nsv3922777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 73,879,477-93,189,581 , NCBI36 chr12: 72,165,744-91,713,712 , GRCh38 chr12: 73,485,697-92,795,805	DCN, RN7SL734P, 195 more genes
nsv4456763	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 77,737,623-94,330,526 , GRCh38.p12 chr12: 77,343,843-93,936,750	DCN, MIR1252, 162 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	DCN, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	DCN, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	DCN, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	DCN, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	DCN, OR5BT1P, 2441 more genes
nsv3924338	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 89,962,226-108,055,398 , GRCh38 chr12: 91,044,318-109,133,210 , GRCh37 chr12: 91,438,095-109,571,015	DCN, NUP37, 295 more genes
nsv3911770	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr12: 89,914,416-93,790,725 , GRCh37 chr12: 91,390,285-95,266,594 , GRCh38 chr12: 90,996,508-94,872,818	DCN, BTG1, 63 more genes
nsv3905832	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 91,352,710-91,776,390 , GRCh38.p12 chr12: 90,958,933-91,382,613	DCN, EPYC, 5 more genes
nsv3892392	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 90,881,837-91,582,957 , GRCh38.p12 chr12: 90,488,060-91,189,180	DCN, EPYC, 6 more genes
nsv3906913	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 87,654,236-91,893,923 , GRCh38.p12 chr12: 87,260,459-91,500,146	DCN, ATP2B1, 53 more genes
nsv6313949	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 91,073,628-92,829,926 , GRCh38.p12 chr12: 90,679,851-92,436,150	DCN, LOC105369896, 20 more genes
nsv3904992	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 90,910,083-91,560,392 , GRCh38.p12 chr12: 90,516,306-91,166,615	DCN, KERA, 6 more genes
nsv3920080	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 89,115,205-90,156,912 , GRCh38 chr12: 90,197,297-91,239,004 , GRCh37 chr12: 90,591,074-91,632,781	DCN, KERA, 8 more genes
nsv4729322	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 90,629,021-91,543,515 , GRCh38.p12 chr12: 90,235,244-91,149,738	DCN, LINC00615, 8 more genes

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