1-0653-001 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
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
nsv4383565	copy number variation	81	nstd173	human		GRCh37 chr11: 7,813,027-7,837,000 , GRCh38.p12 chr11: 7,791,480-7,815,453 , GRCh38.p12 chr11\|NT_187583.1: 12,348-36,321 , GRCh38.p12 chr11\|NW_011332695.1: 12,348-36,332	OR5P2
nsv4385079	copy number variation	34	nstd173	human		GRCh37 chr2: 98,141,300-98,162,176 , GRCh38.p12 chr2: 97,524,837-97,545,713	ANKRD36B
nsv4369174	copy number variation	21	nstd173	human		GRCh37 chr2: 130,817,326-130,878,657 , GRCh38.p12 chr2: 130,059,753-130,121,084	POTEF, POTEF-AS1, 1 more genes
nsv4370901	copy number variation	1	nstd173	human		GRCh37 chr12: 57,335,468-57,378,349 , GRCh38.p12 chr12: 56,941,684-56,984,565	RDH16, LOC390332, 1 more genes
nsv4368906	copy number variation	11	nstd173	human		GRCh37 chr6: 254,283-294,923 , GRCh38.p12 chr6: 254,283-294,923	, DUSP22, 1 more genes
nsv4373673	copy number variation	1	nstd173	human		GRCh37 chr20: 44,371,922-44,395,696 , GRCh38.p12 chr20: 45,743,283-45,767,057	WFDC3, SPINT5P, 1 more genes
nsv4372921	copy number variation	4	nstd173	human		GRCh37 chr11: 55,374,135-55,435,179 , GRCh38.p12 chr11: 55,606,659-55,667,703	OR4S2, OR4P4, 1 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
nsv4373711	copy number variation	238	nstd173	human		GRCh37 chr14: 74,001,111-74,031,034 , GRCh38.p12 chr14: 73,534,407-73,564,330	NT5CP2, HEATR4, 1 more genes
nsv4369186	copy number variation	2	nstd173	human		GRCh37 chrX: 98,713,494-98,860,140 , GRCh38.p12 chrX: 99,458,496-99,605,142	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
nsv4382674	copy number variation	34	nstd173	human		GRCh37 chr2: 4,208,245-4,235,384 , GRCh38.p12 chr2: 4,160,655-4,187,794	0
nsv4376219	copy number variation	2	nstd173	human		GRCh37 chr14: 22,607,782-22,970,492 , GRCh38.p12 chr14: 22,139,819-22,501,508	TRDV3, TRAJ44, 55 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
nsv4369698	copy number variation	12	nstd173	human		GRCh37 chr11: 37,754,660-37,834,730 , GRCh38.p12 chr11: 37,733,110-37,813,180	0
nsv4374831	copy number variation	35	nstd173	human		GRCh37 chr7: 38,319,296-38,378,483 , GRCh38.p12 chr7: 38,279,695-38,338,882	TRGV9, TRGV6, 9 more genes
nsv4372589	copy number variation	741	nstd173	human		GRCh37 chr14: 106,530,472-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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