OCD93-JW-1412 AND nstd173 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4387403	copy number variation	1	nstd173	human		GRCh37 chrX: 321,857-387,749 , GRCh38.p12 chrX: 361,122-427,014 , GRCh38.p12 chrX\|NT_187667.1: 33,615-99,507 , GRCh38.p12 chrX\|NT_187634.1: 44,475-110,367	PPP2R3B
nsv4387213	copy number variation	434	nstd173	human		GRCh37 chr4: 34,779,032-34,824,730 , GRCh38.p12 chr4: 34,777,410-34,823,108 , GRCh38.p12 chr4\|NW_003315915.1: 269,739-315,437	LOC105378262
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
nsv4386429	copy number variation	124	nstd173	human		GRCh37 chr13: 57,758,276-57,778,379 , GRCh38.p12 chr13: 57,184,142-57,204,245	MTCO2P3
nsv4385455	copy number variation	190	nstd173	human		GRCh37 chr20: 1,557,177-1,597,997 , GRCh38.p12 chr20: 1,576,531-1,617,351	SIRPB1
nsv4375924	copy number variation	2	nstd173	human		GRCh37 chr7: 75,349,268-75,378,568 , GRCh38.p12 chr7: 75,719,950-75,749,250	HIP1
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
nsv4370464	copy number variation	362	nstd173	human		GRCh37 chr11: 4,967,239-4,991,060 , GRCh38.p12 chr11: 4,946,009-4,969,830	OR51A4, OR51A2
nsv4375779	copy number variation	6	nstd173	human		GRCh37 chr22: 25,726,674-25,922,334 , GRCh38.p12 chr22: 25,330,707-25,526,367	CRYBB2P1, LRP5L, 2 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
nsv4384272	copy number variation	1	nstd173	human		GRCh37 chr15: 43,889,913-43,976,419 , GRCh38.p12 chr15: 43,597,715-43,684,221	CKMT1B, CATSPER2, 6 more genes
nsv4365127	copy number variation	1	nstd173	human		GRCh37 chr14: 106,880,556-106,924,693 , GRCh38.p12 chr14: 106,424,650-106,468,769 , GRCh38.p12 chr14\|NT_187600.1: 916,329-960,448	IGH, IGHVII-40-1, 5 more genes
nsv4388178	copy number variation	10	nstd173	human		GRCh37 chr5: 120,674,264-120,709,623 , GRCh38.p12 chr5: 121,338,569-121,373,928	0
nsv4377622	copy number variation	1	nstd173	human		GRCh37 chr14: 22,643,556-22,943,215 , GRCh38.p12 chr14: 22,175,659-22,474,225	TRDV3, TRDJ4, 28 more genes
nsv4370946	copy number variation	301	nstd173	human		GRCh37 chr16: 34,466,691-34,755,828 , GRCh38.p12 chr16: 35,232,320-35,521,457	RARRES2P7, AGGF1P9, 26 more genes
nsv4372139	copy number variation	9	nstd173	human		GRCh37 chr14: 106,525,299-106,693,442 , GRCh38.p12 chr14: 106,069,054-106,236,829 , GRCh38.p12 chr14\|NT_187600.1: 536,823-704,598	IGHV3-11, IGHVII-20-1, 19 more genes
nsv4385533	copy number variation	9	nstd173	human		GRCh37 chr7: 38,295,932-38,391,352 , GRCh38.p12 chr7: 38,256,331-38,351,751	TRGV8, TRGV5P, 19 more genes

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