1-0600-004 AND nstd173 - dbVar - NCBI

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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
nsv4382648	copy number variation	8	nstd173	human		GRCh37 chr6: 294,713-381,137 , GRCh38.p12 chr6: 294,713-381,137	DUSP22
nsv4376284	copy number variation	379	nstd173	human		GRCh37 chr14: 41,608,616-41,657,457 , GRCh38.p12 chr14: 41,139,413-41,188,254	LINC02315
nsv4378898	copy number variation	1	nstd173	human		GRCh37 chr6: 101,945,711-101,989,585 , GRCh38.p12 chr6: 101,497,835-101,541,709	GRIK2
nsv4377437	copy number variation	30	nstd173	human		GRCh37 chr9: 6,689,709-6,712,314 , GRCh38.p12 chr9: 6,689,709-6,712,314	LINC02851
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
nsv4381481	copy number variation	1	nstd173	human		GRCh37 chr8: 4,946,863-5,023,482 , GRCh38.p12 chr8: 5,089,341-5,165,960	LOC107986907, RN7SL318P
nsv4380251	copy number variation	13	nstd173	human		GRCh37 chr19: 41,345,327-41,392,653 , GRCh38.p12 chr19: 40,839,422-40,886,748	CYP2A7, CYP2A6
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
nsv4367541	copy number variation	7	nstd173	human		GRCh37 chr5: 17,602,612-17,654,787 , GRCh38.p12 chr5: 17,602,503-17,654,678	H3Y1, H3P20, 3 more genes
nsv4387268	copy number variation	45	nstd173	human		GRCh37 chr12: 11,220,827-11,251,861 , GRCh38.p12 chr12: 11,068,228-11,099,262	PRH1, TAS2R43, 3 more genes
nsv4375659	copy number variation	94	nstd173	human		GRCh37 chr11: 55,374,019-55,435,179 , GRCh38.p12 chr11: 55,606,543-55,667,703	OR4P4, OR4S2, 1 more genes
nsv4376391	copy number variation	14	nstd173	human		GRCh37 chr14: 22,854,897-22,896,881 , GRCh38.p12 chr14: 22,386,494-22,427,889	TRD, TRA, 2 more genes
nsv4375373	copy number variation	3	nstd173	human		GRCh37 chr2: 52,738,983-52,790,246 , GRCh38.p12 chr2: 52,511,845-52,563,108	0
nsv4387125	copy number variation	432	nstd173	human		GRCh37 chr2: 35,967,123-35,997,473 , GRCh38.p12 chr2: 35,742,057-35,772,407	0
nsv4374737	copy number variation	5	nstd173	human		GRCh37 chr1: 41,346,790-41,375,149 , GRCh38.p12 chr1: 40,881,118-40,909,477	0

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