1-0702-004 AND nstd173 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4365613	copy number variation	1	nstd173	human		GRCh37 chr11: 84,530,513-84,596,118 , GRCh38.p12 chr11: 84,819,470-84,885,074	DLG2
nsv4380915	copy number variation	14	nstd173	human		GRCh37 chr11: 49,708,362-49,758,260 , GRCh38.p12 chr11: 49,686,810-49,736,708 , GRCh38.p12 chr11\|NW_019805495.1: 150,992-200,857	GRM5P1
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
nsv4369954	copy number variation	20	nstd173	human		GRCh37 chr20: 14,781,684-14,823,472 , GRCh38.p12 chr20: 14,801,038-14,842,826	MACROD2
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
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
nsv4365971	copy number variation	432	nstd173	human		GRCh37 chr1: 248,753,196-248,795,289 , GRCh38.p12 chr1: 248,589,895-248,631,988	OR2T10, OR2T11
nsv4382253	copy number variation	206	nstd173	human		GRCh37 chr12: 11,503,225-11,553,849 , GRCh38.p12 chr12: 11,350,291-11,400,915 , GRCh38.p12 chr12\|NT_187658.1: 545,254-572,349	PRB2, PRB1
nsv4379551	copy number variation	16	nstd173	human		GRCh37 chr11: 55,402,801-55,452,996 , GRCh38.p12 chr11: 55,635,325-55,685,520	OR4C6, OR4V1P, 3 more genes
nsv4377906	copy number variation	34	nstd173	human		GRCh37 chr5: 180,378,754-180,416,782 , GRCh38.p12 chr5: 180,951,754-180,989,782	BTNL8, ARPP19P1, 3 more genes
nsv4375644	copy number variation	145	nstd173	human		GRCh37 chr22: 25,656,238-25,922,334 , GRCh38.p12 chr22: 25,260,271-25,526,367	CRYBB2P1, IGLL3P, 4 more genes
nsv4377506	copy number variation	5	nstd173	human		GRCh37 chr6: 67,009,023-67,051,154 , GRCh38.p12 chr6: 66,299,130-66,341,261	0
nsv4369278	copy number variation	284	nstd173	human		GRCh37 chrX: 115,133,389-115,156,164 , GRCh38.p12 chr: NaN-NaN	0
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0
nsv4370479	copy number variation	32	nstd173	human		GRCh37 chr7: 43,361-65,578 , GRCh38.p12 chr7: 43,361-65,578 , GRCh38.p12 chr7\|NT_187558.1: 1-21,677 , GRCh38.p12 chr7\|NT_187653.1: 35,682-57,899	0

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