2-1182-001 AND nstd173 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4386181	copy number variation	2	nstd173	human		GRCh37 chr16: 80,896,302-80,955,393 , GRCh38.p12 chr16: 80,862,405-80,921,496	ARLNC1
nsv4374777	copy number variation	2	nstd173	human		GRCh37 chr19: 41,360,130-41,385,370 , GRCh38.p12 chr19: 40,854,225-40,879,465	CYP2A7
nsv4376456	copy number variation	1782	nstd173	human		GRCh37 chr8: 39,246,772-39,386,964 , GRCh38.p12 chr8: 39,389,253-39,529,445	ADAM5, ADAM3A
nsv4367575	copy number variation	1	nstd173	human		GRCh37 chr21: 43,849,380-43,913,089 , GRCh38.p12 chr21: 42,429,271-42,492,979	RSPH1, UBASH3A
nsv4376723	copy number variation	40	nstd173	human		GRCh37 chr12: 8,558,475-8,584,702 , GRCh38.p12 chr12: 8,405,879-8,432,106	OR7E140P, OR7E148P
nsv4377875	copy number variation	73	nstd173	human		GRCh37 chr5: 180,375,302-180,430,797 , GRCh38.p12 chr5: 180,948,302-181,003,797	BTNL8, BTNL3, 3 more genes
nsv4376452	copy number variation	337	nstd173	human		GRCh37 chr17: 34,437,494-34,477,480 , GRCh38.p12 chr17: 36,110,101-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 64,198-104,195 , GRCh38.p12 chr17\|NT_187614.1: 345,022-385,008	LOC101927369, LOC107985055, 3 more genes
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 3 more genes
nsv4379682	copy number variation	1	nstd173	human		GRCh37 chr12: 127,507,099-127,785,576 , GRCh38.p12 chr12: 127,022,554-127,301,031 , GRCh38.p12 chr12\|NW_019805499.1: 1-154,139	LINC02405, LOC105370062, 5 more genes
nsv4368892	copy number variation	173	nstd173	human		GRCh37 chr14: 106,530,472-106,693,442 , GRCh38.p12 chr14: 106,074,229-106,236,829 , GRCh38.p12 chr14\|NT_187600.1: 541,998-704,598	LOC105370700, IGHV3-19, 19 more genes
nsv4367492	copy number variation	84	nstd173	human		GRCh37 chr4: 161,041,291-161,080,636 , GRCh38.p12 chr4: 160,120,139-160,159,484	0
nsv4371608	copy number variation	1	nstd173	human		GRCh37 chr9: 4,339,193-4,361,797 , GRCh38.p12 chr9: 4,339,193-4,361,797	0
nsv4384501	copy number variation	242	nstd173	human		GRCh37 chr16: 19,945,795-19,965,942 , GRCh38.p12 chr16: 19,934,473-19,954,620	0
nsv4373909	copy number variation	3	nstd173	human		GRCh37 chr14: 107,150,444-107,179,546 , GRCh38.p12 chr14: 106,694,427-106,771,304	IGH, IGHVIII-67-4, 7 more genes

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