11-0041-003 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
nsv4368347	copy number variation	1	nstd173	human		GRCh37 chr9: 7,818,894-8,041,879 , GRCh38.p12 chr9: 7,818,894-8,041,879	LOC105375971
nsv4376255	copy number variation	343	nstd173	human		GRCh37 chr2: 98,118,199-98,162,176 , GRCh38.p12 chr2: 97,501,736-97,545,713	ANKRD36B
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
nsv4378486	copy number variation	188	nstd173	human		GRCh37 chr1: 248,753,184-248,795,289 , GRCh38.p12 chr1: 248,589,883-248,631,988	OR2T10, OR2T11
nsv4372305	copy number variation	7	nstd173	human		GRCh37 chr3: 35,800,767-35,949,450 , GRCh38.p12 chr3: 35,759,275-35,907,958	ARPP21, RPL36AP17
nsv4383512	copy number variation	15	nstd173	human		GRCh37 chr19: 53,517,242-53,547,172 , GRCh38.p12 chr19: 53,013,989-53,043,919	ERVV-1, ERVV-2
nsv4379351	copy number variation	123	nstd173	human		GRCh37 chr19: 51,321,391-51,345,568 , GRCh38.p12 chr19: 50,818,135-50,842,312	LOC105372441, KLK1, 2 more genes
nsv4370796	copy number variation	34	nstd173	human		GRCh37 chr5: 180,375,290-180,430,789 , GRCh38.p12 chr5: 180,948,290-181,003,789	LOC100128762, TMEM69P2, 3 more genes
nsv4383617	copy number variation	2	nstd173	human		GRCh37 chr1: 1,627,905-1,672,591 , GRCh38.p12 chr1: 1,696,466-1,741,152	MMP23A, CDK11A, 2 more genes
nsv4375017	copy number variation	2	nstd173	human		GRCh37 chr5: 17,513,397-17,654,787 , GRCh38.p12 chr5: 17,513,288-17,654,678	TAF11L4, TAF11L6, 7 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
nsv4367492	copy number variation	84	nstd173	human		GRCh37 chr4: 161,041,291-161,080,636 , GRCh38.p12 chr4: 160,120,139-160,159,484	0
nsv4373957	copy number variation	1	nstd173	human		GRCh37 chr2: 10,657,725-10,913,984 , GRCh38.p12 chr2: 10,517,599-10,773,858	ATP6V1C2, NOL10, 4 more genes
nsv4369404	copy number variation	213	nstd173	human		GRCh37 chr14: 107,150,444-107,179,594 , GRCh38.p12 chr14: 106,694,427-106,771,352	IGHV2-70, IGH, 7 more genes
nsv4383665	copy number variation	9	nstd173	human		GRCh37 chr14: 22,404,167-22,977,816 , GRCh38.p12 chr14: 21,935,993-22,508,831	TRAV41, TRAJ38, 79 more genes
nsv4369196	copy number variation	1	nstd173	human		GRCh37 chr7: 142,342,271-142,486,483 , GRCh38.p12 chr7: 142,634,755-142,778,673 , GRCh38.p12 chr7\|NT_187562.1: 656,734-781,128	PRSS1, TRBV26, 17 more genes
nsv4371117	copy number variation	49	nstd173	human		GRCh37 chr7: 38,294,088-38,394,857 , GRCh38.p12 chr7: 38,254,487-38,355,256	TRGVA, TRGC1, 19 more genes
nsv4368473	copy number variation	289	nstd173	human		GRCh37 chr22: 42,918,351-42,943,641 , GRCh38.p12 chr22: 42,522,345-42,547,635	0
nsv4374014	copy number variation	33	nstd173	human		GRCh37 chr5: 57,326,267-57,349,986 , GRCh38.p12 chr5: 58,030,440-58,054,159	0

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