166508 AND nstd173 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4365918	copy number variation	1	nstd173	human		GRCh37 chr8: 71,614,663-71,662,428 , GRCh38.p12 chr8: 70,702,428-70,750,193	XKR9
nsv4369339	copy number variation	1	nstd173	human		GRCh37 chr16: 84,420,341-84,443,412 , GRCh38.p12 chr16: 84,386,735-84,409,806	ATP2C2
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
nsv4375646	copy number variation	78	nstd173	human		GRCh37 chr1: 72,762,663-72,810,925 , GRCh38.p12 chr1: 72,296,980-72,345,242 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-66,467	LOC105378797, RPL31P12
nsv4381562	copy number variation	367	nstd173	human		GRCh37 chr11: 55,374,019-55,453,008 , GRCh38.p12 chr11: 55,606,543-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4375662	copy number variation	272	nstd173	human		GRCh37 chr11: 5,783,910-5,809,230 , GRCh38.p12 chr11: 5,762,680-5,788,000	OR52N1, OR56B2P, 1 more genes
nsv4376100	copy number variation	22	nstd173	human		GRCh37 chr22: 18,916,843-19,004,772 , GRCh38.p12 chr22: 18,929,330-19,017,259	PRODH, DGCR5
nsv4387125	copy number variation	432	nstd173	human		GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407	0
nsv4373715	copy number variation	1	nstd173	human		GRCh37 chr14: 22,462,737-22,970,223 , GRCh38.p12 chr14: 21,994,497-22,501,239	TRAJ49, TRAJ46, 68 more genes
nsv4367417	copy number variation	12	nstd173	human		GRCh37 chr7: 38,295,932-38,356,732 , GRCh38.p12 chr7: 38,256,331-38,317,131	TARP, TRGJP1, 11 more genes
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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