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

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4729473	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 86,223,018-86,302,962 , GRCh38.p12 chr12: 85,829,240-85,909,184	NTS, RASSF9
nsv4729575	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr12: 86,017,618-86,786,974 , GRCh38.p12 chr12: 85,623,840-86,393,196	NTS, LOC105369877, 3 more genes
nsv3909921	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr12: 85,722,164-86,332,192 , NCBI36 chr12: 84,640,073-85,250,101 , GRCh37 chr12: 86,115,942-86,725,970	NTS, RASSF9, 3 more genes
nsv4675611	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 86,173,243-86,421,728 , GRCh38.p12 chr12: 85,779,465-86,027,950	NTS, MGAT4C, 2 more genes
nsv3892030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 69,608,090-89,629,345 , GRCh38.p12 chr12: 69,214,310-89,235,568	NTS, LOC101928002, 197 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	NTS, 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	NTS, 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	NTS, 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	NTS, 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	NTS, 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	NTS, 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	NTS, OR5BT1P, 2441 more genes
nsv4348838	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 82,183,041-88,755,577 , GRCh38.p12 chr12: 81,789,262-88,361,800	NTS, LOC101059974, 47 more genes
nsv3898204	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 86,115,942-88,186,381 , GRCh38.p12 chr12: 85,722,164-87,792,604	NTS, LOC105369880, 13 more genes
nsv4455384	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 86,138,213-88,183,106 , GRCh38.p12 chr12: 85,744,435-87,789,329	NTS, LOC107984478, 13 more genes
nsv4729086	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 85,812,496-86,797,077 , GRCh38.p12 chr12: 85,418,718-86,403,299	NTS, LOC101059974, 6 more genes

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