1-0449-002 AND nstd173 - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4376790	copy number variation	30	nstd173	human		GRCh37 chr11: 49,708,362-49,757,670 , GRCh38.p12 chr11: 49,686,810-49,736,118 , GRCh38.p12 chr11\|NW_019805495.1: 150,992-200,267	GRM5P1
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
nsv4383903	copy number variation	5	nstd173	human		GRCh37 chr2: 52,378,299-52,399,270 , GRCh38.p12 chr2: 52,151,161-52,172,132	NRXN1-DT
nsv4375513	copy number variation	189	nstd173	human		GRCh37 chr1: 72,771,354-72,812,440 , GRCh38.p12 chr1: 72,305,671-72,346,757 , GRCh38.p12 chr1\|NW_018654707.1: 17,938-67,982	LOC105378797
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4366274	copy number variation	133	nstd173	human		GRCh37 chr7: 75,354,113-75,375,909 , GRCh38.p12 chr7: 75,724,795-75,746,591	HIP1
nsv4365971	copy number variation	432	nstd173	human		GRCh37 chr1: 248,753,196-248,795,289 , GRCh38.p12 chr1: 248,589,895-248,631,988	OR2T10, OR2T11
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 more genes
nsv4366631	copy number variation	46	nstd173	human		GRCh37 chr12: 11,220,827-11,256,413 , GRCh38.p12 chr12: 11,068,228-11,103,814	PRH1, TAS2R64P, 3 more genes
nsv4367271	copy number variation	561	nstd173	human		GRCh37 chr11: 5,786,020-5,809,230 , GRCh38.p12 chr11: 5,764,790-5,788,000	OR56B2P, OR52N1, 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
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
nsv4375644	copy number variation	145	nstd173	human		GRCh37 chr22: 25,656,238-25,922,334 , GRCh38.p12 chr22: 25,260,271-25,526,367	CRYBB2P1, IGLL3P, 4 more genes
nsv4386797	copy number variation	1	nstd173	human		GRCh37 chrX: 768,139-837,407 , GRCh38.p12 chrX: 807,404-876,672	0
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

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1-0449-002 AND nstd173 (16)
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