1-0375-002 AND nstd173 - dbVar - NCBI

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Items: 19

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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
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
nsv4375716	copy number variation	91	nstd173	human		GRCh37 chr3: 165,041,535-165,085,386 , GRCh38.p12 chr3: 165,323,747-165,367,598	LINC01322
nsv4370897	copy number variation	108	nstd173	human		GRCh37 chr13: 57,758,269-57,778,367 , GRCh38.p12 chr13: 57,184,135-57,204,233	MTCO2P3
nsv4376119	copy number variation	1	nstd173	human		GRCh37 chr3: 2,285,496-2,760,756 , GRCh38.p12 chr3: 2,243,812-2,719,072	CNTN4, HINT2P1
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
nsv4381433	copy number variation	68	nstd173	human		GRCh37 chr1: 196,827,842-196,877,049 , GRCh38.p12 chr1: 196,858,712-196,907,919	LOC100996886, CFHR4
nsv4367885	copy number variation	14	nstd173	human		GRCh37 chr19: 53,517,242-53,547,361 , GRCh38.p12 chr19: 53,013,989-53,044,108	ERVV-1, ERVV-2
nsv4388035	copy number variation	283	nstd173	human		GRCh37 chr1: 104,109,088-104,132,506 , GRCh38.p12 chr1: 103,566,466-103,589,884	AMY2B, ACTG1P4
nsv4376100	copy number variation	22	nstd173	human		GRCh37 chr22: 18,916,843-19,004,772 , GRCh38.p12 chr22: 18,929,330-19,017,259	PRODH, DGCR5
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
nsv4385218	copy number variation	5	nstd173	human		GRCh37 chr6: 254,254-290,585 , GRCh38.p12 chr6: 254,254-290,585	, , 1 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
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
nsv4368087	copy number variation	16	nstd173	human		GRCh37 chr11: 55,363,327-55,453,008 , GRCh38.p12 chr11: 55,595,851-55,685,532	OR4V1P, OR4C11, 4 more genes
nsv4372155	copy number variation	28	nstd173	human		GRCh37 chr5: 180,378,754-180,442,387 , GRCh38.p12 chr5: 180,951,754-181,015,387	ARPP19P1, BTNL3, 4 more genes
nsv4381952	copy number variation	1	nstd173	human		GRCh37 chr6: 33,222,841-33,259,562 , GRCh38.p12 chr6: 33,255,064-33,291,785	RGL2, VPS52, 7 more genes
nsv4369508	copy number variation	1	nstd173	human		GRCh37 chr7: 38,290,714-38,319,464 , GRCh38.p12 chr7: 38,251,113-38,279,863	TRGJP, TRGJP1, 7 more genes
nsv4387224	copy number variation	1	nstd173	human		GRCh37 chr14: 22,792,993-22,942,890 , GRCh38.p12 chr14: 22,324,561-22,473,900	TRAJ61, TRDD1, 14 more genes

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