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

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3922675	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 22,519,683-25,226,559 , NCBI36 chr6: 22,627,662-25,334,538 , GRCh38 chr6: 22,519,454-25,226,331	PPIAP29, ACOT13, 42 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	LOC105378061, MIR4640, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	RNU6-411P, LOC107986611, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SOD1P1, HLA-DPB1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ITPR3, HSD17B8, 2905 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	TRR-ACG1-2, TMEM217, 1385 more genes
nsv3920564	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 3,224,310-30,657,190 , GRCh37 chr6: 3,224,544-30,624,967 , NCBI36 chr6: 3,169,543-30,732,946	PRELID1P2, RPL7AP7, 785 more genes
nsv3922819	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 23,360,729-26,075,484 , GRCh37 chr6: 23,252,750-25,967,505 , GRCh38 chr6: 23,252,522-25,967,277	KAAG1, ACOT13, 52 more genes
nsv4675407	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 24,497,678-25,168,510 , GRCh38.p12 chr6: 24,497,450-25,168,282	C6orf62, AP3S1P1, 18 more genes

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