168209 AND nstd173 - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4380946	copy number variation	14	nstd173	human		GRCh37 chr17: 36,350,006-36,404,136 , GRCh38.p12 chr17\|NT_187614.1: 2,229,071-2,283,201	NPEPPSP1
nsv4367943	copy number variation	4	nstd173	human		GRCh37 chr11: 49,710,692-49,760,797 , GRCh38.p12 chr11: 49,689,140-49,739,245 , GRCh38.p12 chr11\|NW_019805495.1: 153,322-203,394	GRM5P1
nsv4375513	copy number variation	189	nstd173	human		GRCh37 chr1: 72,771,354-72,812,440 , GRCh38.p12 chr1: 72,305,671-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,938-67,982	LOC105378797
nsv4374127	copy number variation	3	nstd173	human		GRCh37 chr3: 173,239,853-173,289,679 , GRCh38.p12 chr3: 173,522,063-173,571,889	NLGN1
nsv4387053	copy number variation	81	nstd173	human		GRCh37 chr6: 124,432,055-124,470,365 , GRCh38.p12 chr6: 124,110,910-124,149,220	NKAIN2
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
nsv4372309	copy number variation	2	nstd173	human		GRCh37 chr7: 62,437,464-62,660,019 , GRCh38.p12 chr7: 62,977,086-63,199,641	ZNF90P3, LOC100419991, 3 more genes
nsv4372368	copy number variation	31	nstd173	human		GRCh37 chr4: 69,435,889-69,541,894 , GRCh38.p12 chr4: 68,570,171-68,676,176	LOC728807, UGT2B15, 3 more genes
nsv4376806	copy number variation	247	nstd173	human		GRCh37 chr12: 11,219,930-11,247,388 , GRCh38.p12 chr12: 11,067,331-11,094,789	PRH1, PRH1-PRR4, 3 more genes
nsv4373540	copy number variation	34	nstd173	human		GRCh37 chr19: 20,598,430-20,720,705 , GRCh38.p12 chr19: 20,415,624-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4383655	copy number variation	30	nstd173	human		GRCh37 chr11: 54,965,375-55,009,349 , GRCh38.p12 chr11: 55,197,899-55,241,873	0
nsv4369278	copy number variation	284	nstd173	human		GRCh37 chrX: 115,133,389-115,156,164 , GRCh38.p12 chr: NaN-NaN	0
nsv4371406	copy number variation	8	nstd173	human		GRCh37 chr6: 110,394,605-110,415,232 , GRCh38.p12 chr6: 110,073,402-110,094,029	0
nsv4385718	copy number variation	16	nstd173	human		GRCh37 chr16: 19,945,807-19,965,942 , GRCh38.p12 chr16: 19,934,485-19,954,620	0
nsv4383947	copy number variation	1	nstd173	human		GRCh37 chrX: 168,547-471,180 , GRCh38.p12 chrX: 251,880-510,445 , GRCh38.p12 chrX\|NT_187667.1: 25,947-182,938 , GRCh38.p12 chrX\|NT_187634.1: 37,893-193,798	PLCXD1, LINC00685, 4 more genes
nsv4370832	copy number variation	1	nstd173	human		GRCh37 chr14: 22,387,771-22,970,492 , GRCh38.p12 chr14: 21,919,596-22,501,508	TRAJ58, TRAV20, 74 more genes
nsv4387089	copy number variation	69	nstd173	human		GRCh37 chr7: 142,342,271-142,493,638 , GRCh38.p12 chr7: 142,634,755-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	TRBV21-1, TRB, 21 more genes
nsv4386651	copy number variation	6	nstd173	human		GRCh37 chr7: 38,294,983-38,386,791 , GRCh38.p12 chr7: 38,255,382-38,347,190	TRGJP, TRGVB, 17 more genes
nsv4378798	copy number variation	1	nstd173	human		GRCh37 chrX: 58,504,117-58,527,164 , GRCh38.p12 chrX: 58,477,684-58,500,731	0

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