1-0772-003 AND nstd173 - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4377496	copy number variation	1	nstd173	human		GRCh37 chr11: 49,710,849-49,760,688 , GRCh38.p12 chr11: 49,689,297-49,739,136 , GRCh38.p12 chr11\|NW_019805495.1: 153,479-203,285	GRM5P1
nsv4371805	copy number variation	282	nstd173	human		GRCh37 chr11: 18,941,197-18,961,975 , GRCh38.p12 chr11: 18,919,650-18,940,428	MRGPRX1
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
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
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
nsv4367036	copy number variation	2	nstd173	human		GRCh37 chrX: 134,754,594-134,802,994 , GRCh38.p12 chrX: 135,620,669-135,669,279	SAGE4P, SAGE3P
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
nsv4381102	copy number variation	1	nstd173	human		GRCh37 chr6: 10,460,872-10,531,003 , GRCh38.p12 chr6: 10,460,639-10,530,770 , GRCh38.p12 chr6\|NW_018654713.1: 1-41,654	LINC02522, LOC101928146, 3 more genes
nsv4374780	copy number variation	6	nstd173	human		GRCh37 chr11: 55,363,327-55,435,179 , GRCh38.p12 chr11: 55,595,851-55,667,703	OR4P4, OR4S2, 2 more genes
nsv4372487	copy number variation	231	nstd173	human		GRCh37 chr12: 11,219,930-11,251,705 , GRCh38.p12 chr12: 11,067,331-11,099,106	TAS2R64P, PRH1, 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
nsv4383655	copy number variation	30	nstd173	human		GRCh37 chr11: 54,965,375-55,009,349 , GRCh38.p12 chr11: 55,197,899-55,241,873	0
nsv4378968	copy number variation	1	nstd173	human		GRCh37 chr9: 12,853,276-12,886,617 , GRCh38.p12 chr9: 12,853,277-12,886,618	0
nsv4376526	copy number variation	4	nstd173	human		GRCh37 chr4: 10,209,966-10,240,060 , GRCh38.p12 chr4: 10,208,342-10,238,436	0
nsv4382392	copy number variation	421	nstd173	human		GRCh37 chr3: 65,185,849-65,210,375 , GRCh38.p12 chr3: 65,200,174-65,224,700	0
nsv4367819	copy number variation	2	nstd173	human		GRCh37 chr3: 175,892,129-175,916,315 , GRCh38.p12 chr3: 176,174,341-176,198,527 , GRCh38.p12 chr3\|NW_019805488.1: 58,852-83,038	0
nsv4370058	copy number variation	1	nstd173	human		GRCh37 chr16: 21,581,218-21,841,354 , GRCh38.p12 chr16: 21,569,897-21,830,033 , GRCh38.p12 chr16\|NW_017852933.1: 1,274,742-1,534,916	RNU6-196P, IGSF6, 6 more genes
nsv4372634	copy number variation	1	nstd173	human		GRCh37 chr6: 13,174,713-13,346,684 , GRCh38.p12 chr6: 13,174,481-13,346,452	TBC1D7, PHACTR1, 4 more genes

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