10-1090-005 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
nsv4372152	copy number variation	236	nstd173	human		GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467	LOC105377865
nsv4380546	copy number variation	2	nstd173	human		GRCh37 chr9: 29,085,572-29,113,616 , GRCh38.p12 chr9: 29,085,574-29,113,618	LINGO2
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4366850	copy number variation	2	nstd173	human		GRCh37 chr3: 89,394,579-89,420,218 , GRCh38.p12 chr3: 89,345,429-89,371,068	EPHA3
nsv4373295	copy number variation	124	nstd173	human		GRCh37 chr13: 69,248,299-69,268,719 , GRCh38.p12 chr13: 68,674,167-68,694,587	RN7SL761P
nsv4371546	copy number variation	1	nstd173	human		GRCh37 chr14: 61,339,139-61,366,019 , GRCh38.p12 chr14: 60,872,421-60,899,301	MNAT1
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
nsv4372080	copy number variation	569	nstd173	human		GRCh37 chr1: 72,762,663-72,812,440 , GRCh38.p12 chr1: 72,296,980-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,982	RPL31P12, LOC105378797
nsv4383109	copy number variation	49	nstd173	human		GRCh37 chr11: 55,374,031-55,453,575 , GRCh38.p12 chr11: 55,606,555-55,686,099	OR4P1P, OR4P4, 3 more genes
nsv4375958	copy number variation	2	nstd173	human		GRCh37 chr1: 1,616,990-1,652,775 , GRCh38.p12 chr1: 1,685,551-1,721,336	SLC35E2B, CDK11A, 1 more genes
nsv4386886	copy number variation	138	nstd173	human		GRCh37 chr19: 54,730,238-54,752,217 , GRCh38.p12 chr19: 54,226,365-54,248,358 , GRCh38.p12 chr19\|NT_187693.1: 201,352-223,331 , GRCh38.p12 chr19\|NW_003571060.1: 201,350-223,326 , GRCh38.p12 chr19\|NW_003571054.1: 201,165-223,093	LILRB5, LOC100421130, 3 more genes
nsv4374975	copy number variation	1	nstd173	human		GRCh37 chr10: 43,153,955-43,218,552 , GRCh38.p12 chr10: 42,658,507-42,723,104	LINC02632, LINC01518, 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
nsv4366691	copy number variation	623	nstd173	human		GRCh37 chr4: 69,435,901-69,485,978 , GRCh38.p12 chr4: 68,570,183-68,620,260	UGT2B17, LOC100422402, 1 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
nsv4387786	copy number variation	4	nstd173	human		GRCh37 chr5: 45,860,021-45,889,954 , GRCh38.p12 chr5: 45,859,919-45,889,852	0
nsv4387023	copy number variation	344	nstd173	human		GRCh37 chr2: 34,701,643-34,727,784 , GRCh38.p12 chr2: 34,476,576-34,502,717	0
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

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