1-0634-003 AND nstd173 - dbVar - NCBI

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4365923	copy number variation	1	nstd173	human		GRCh37 chr3: 96,285,128-96,318,042 , GRCh38.p12 chr3: 96,566,284-96,599,198	RBBP4P7
nsv4366717	copy number variation	1	nstd173	human		GRCh37 chr4: 69,685,853-69,717,214 , GRCh38.p12 chr4: 68,820,135-68,851,496	UGT2B10
nsv4387073	copy number variation	1	nstd173	human		GRCh37 chr8: 86,382,721-86,533,205 , GRCh38.p12 chr8: 85,470,492-85,620,976	CA2, LOC105375937
nsv4366729	copy number variation	148	nstd173	human		GRCh37 chr8: 39,246,772-39,389,003 , GRCh38.p12 chr8: 39,389,253-39,531,484	ADAM3A, ADAM5
nsv4384822	copy number variation	80	nstd173	human		GRCh37 chr7: 43,361-81,400 , GRCh38.p12 chr7: 43,361-81,400 , GRCh38.p12 chr7\|NT_187558.1: 1-37,499 , GRCh38.p12 chr7\|NT_187653.1: 35,682-73,721	LOC105375113, LOC101929756
nsv4375829	copy number variation	4	nstd173	human		GRCh37 chr11: 89,474,818-89,543,740 , GRCh38.p12 chr11: 89,741,650-89,810,572	TRIM49, TRIM64DP, 2 more genes
nsv4387832	copy number variation	38	nstd173	human		GRCh37 chr12: 11,216,817-11,256,413 , GRCh38.p12 chr12: 11,064,218-11,103,814	TAS2R43, PRH1-TAS2R14, 3 more genes
nsv4374985	copy number variation	188	nstd173	human		GRCh37 chr14: 73,995,761-74,024,031 , GRCh38.p12 chr14: 73,529,057-73,557,327	ACOT1, NT5CP2, 1 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
nsv4368821	copy number variation	1373	nstd173	human		GRCh37 chr22: 24,353,749-24,385,040 , GRCh38.p12 chr22\|NT_187633.1: 247,924-279,215	LOC391322, GSTTP2, 3 more genes
nsv4372664	copy number variation	11	nstd173	human		GRCh37 chr14: 107,150,444-107,173,910 , GRCh38.p12 chr14: 106,694,427-106,718,663	IGH, IGHV1-69, 2 more genes
nsv4377904	copy number variation	28	nstd173	human		GRCh37 chr19: 20,596,118-20,720,868 , GRCh38.p12 chr19: 20,413,312-20,538,062	ZNF826P, ZNF737, 4 more genes
nsv4378133	copy number variation	1	nstd173	human		GRCh37 chr4: 73,709,158-73,756,559 , GRCh38.p12 chr4: 72,843,441-72,890,842	0
nsv4374875	copy number variation	271	nstd173	human		GRCh37 chr6: 67,009,023-67,051,189 , GRCh38.p12 chr6: 66,299,130-66,341,296	0
nsv4369166	copy number variation	31	nstd173	human		GRCh37 chr8: 13,611,631-13,652,975 , GRCh38.p12 chr8: 13,754,122-13,795,466	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4380373	copy number variation	1	nstd173	human		GRCh37 chr14: 22,731,015-22,944,507 , GRCh38.p12 chr14: 22,263,131-22,475,517	TRAJ60, LOC107984649, 23 more genes
nsv4376474	copy number variation	1	nstd173	human		GRCh37 chr7: 22,098,105-22,142,073 , GRCh38.p12 chr7: 22,058,487-22,102,455	0

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