OCD119-S_1725 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
nsv4379044	copy number variation	44	nstd173	human		GRCh37 chr20: 1,560,549-1,593,836 , GRCh38.p12 chr20: 1,579,903-1,613,190	SIRPB1
nsv4385629	copy number variation	207	nstd173	human		GRCh37 chr16: 55,796,376-55,822,431 , GRCh38.p12 chr16: 55,762,464-55,788,519	CES1P1
nsv4375321	copy number variation	4	nstd173	human		GRCh37 chr1: 169,233,973-169,255,389 , GRCh38.p12 chr1: 169,264,735-169,286,151	NME7
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
nsv4368308	copy number variation	37	nstd173	human		GRCh37 chr14: 24,455,412-24,479,697 , GRCh38.p12 chr14: 23,986,203-24,010,488 , GRCh38.p12 chr14\|NW_018654722.1: 273,828-316,310	DHRS4L1, DHRS4L2
nsv4368981	copy number variation	1	nstd173	human		GRCh37 chr22: 18,935,466-19,004,731 , GRCh38.p12 chr22: 18,947,953-19,017,218	DGCR5
nsv4367141	copy number variation	106	nstd173	human		GRCh37 chr5: 32,107,084-32,170,613 , GRCh38.p12 chr5: 32,106,978-32,170,507	PDZD2, GOLPH3
nsv4368478	copy number variation	2	nstd173	human		GRCh37 chr15: 24,357,741-24,504,770 , GRCh38.p12 chr15: 24,112,594-24,259,623	PWRN2, LOC105370732, 1 more genes
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4386906	copy number variation	10	nstd173	human		GRCh37 chr1: 248,688,587-248,794,463 , GRCh38.p12 chr1: 248,525,286-248,631,162	OR2AS1P, OR2T34, 4 more genes
nsv4374692	copy number variation	2	nstd173	human		GRCh37 chr14: 106,072,251-107,285,437 , GRCh38.p12 chr14: 105,786,368-106,877,229 , GRCh38.p12 chr14\|NT_187600.1: 73,683-1,214,078	IGHD4-23, IGHV3-16, 201 more genes
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
nsv4369585	copy number variation	5	nstd173	human		GRCh37 chr6: 103,738,197-103,768,670 , GRCh38.p12 chr6: 103,290,322-103,320,795	0
nsv4387944	copy number variation	45	nstd173	human		GRCh37 chr2: 17,221,307-17,248,504 , GRCh38.p12 chr2: 17,040,040-17,067,237	0
nsv4380168	copy number variation	295	nstd173	human		GRCh37 chr17: 44,187,492-44,784,639 , GRCh38.p12 chr17: 46,110,126-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 812,225-1,226,699	MAPK8IP1P1, DND1P2, 14 more genes
nsv4367920	copy number variation	6	nstd173	human		GRCh37 chr14: 22,457,091-22,974,280 , GRCh38.p12 chr14: 21,988,851-22,505,293	TRAJ38, TRDD1, 72 more genes
nsv4380787	copy number variation	76	nstd173	human		GRCh37 chr7: 38,294,983-38,387,020 , GRCh38.p12 chr7: 38,255,382-38,347,419	TRG, TRGV5P, 18 more genes
nsv4377537	copy number variation	3	nstd173	human		GRCh37 chr7: 142,427,828-142,493,638 , GRCh38.p12 chr7: 142,720,004-142,785,829 , GRCh38.p12 chr7\|NT_187562.1: 734,718-781,128	PGBD4P1, PRSS3P1, 11 more genes
nsv4375229	copy number variation	71	nstd173	human		GRCh37 chr2: 34,701,643-34,723,190 , GRCh38.p12 chr2: 34,476,576-34,498,123	0

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