1-0639-003 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
nsv4379533	copy number variation	1	nstd173	human		GRCh37 chr13: 82,906,859-83,052,149 , GRCh38.p12 chr13: 82,332,724-82,478,014	LOC105370285
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
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
nsv4382544	copy number variation	91	nstd173	human		GRCh37 chr2: 98,138,405-98,162,176 , GRCh38.p12 chr2: 97,521,942-97,545,713	ANKRD36B
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
nsv4375212	copy number variation	547	nstd173	human		GRCh37 chr1: 72,762,663-72,811,904 , GRCh38.p12 chr1: 72,296,980-72,346,221 , GRCh38.p12 chr1\|NW_018654707.1: 9,247-67,446	RPL31P12, LOC105378797
nsv4381562	copy number variation	367	nstd173	human		GRCh37 chr11: 55,374,019-55,453,008 , GRCh38.p12 chr11: 55,606,543-55,685,532	OR4P1P, OR4C6, 3 more genes
nsv4377530	copy number variation	32	nstd173	human		GRCh37 chr22: 39,350,277-39,389,692 , GRCh38.p12 chr22: 38,954,272-38,993,687	LOC105373033, APOBEC3B, 3 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
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
nsv4378105	copy number variation	17	nstd173	human		GRCh37 chr5: 177,227,228-177,250,458 , GRCh38.p12 chr5: 177,800,227-177,823,457	, , 1 more genes
nsv4372687	copy number variation	1	nstd173	human		GRCh37 chr6: 31,359,874-31,456,085 , GRCh38.p12 chr6: 31,392,097-31,488,308	HCP5, HLA-X, 5 more genes
nsv4371210	copy number variation	1	nstd173	human		GRCh37 chr6: 31,952,483-32,028,360 , GRCh38.p12 chr6: 31,984,706-32,060,583	C4A, C4B, 5 more genes
nsv4378128	copy number variation	463	nstd173	human		GRCh37 chr11: 51,337,076-51,376,963 , GRCh38.p12 chr11: 54,742,317-54,782,204	0
nsv4381353	copy number variation	15	nstd173	human		GRCh37 chr13: 69,242,242-69,264,684 , GRCh38.p12 chr13: 68,668,110-68,690,552	0
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4372099	copy number variation	57	nstd173	human		GRCh37 chr17: 34,426,245-34,477,480 , GRCh38.p12 chr17: 36,098,851-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 52,948-104,195 , GRCh38.p12 chr17\|NT_187614.1: 333,773-385,008	LOC100419980, RN7SL301P, 4 more genes
nsv4371194	copy number variation	3	nstd173	human		GRCh37 chr14: 22,643,684-22,974,280 , GRCh38.p12 chr14: 22,175,787-22,505,293	TRAJ45, TRAV26-2, 54 more genes
nsv4380077	copy number variation	1	nstd173	human		GRCh37 chr19: 53,928,751-54,005,308 , GRCh38.p12 chr19: 53,425,498-53,502,054	ZNF761, ZNF813, 8 more genes

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