OSC6390 AND nstd224 - dbVar - NCBI

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Number of Variants: 11

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6628670	copy number variation	44	nstd224	human		GRCh37 chr3: 165,041,791-165,079,776 , GRCh38.p12 chr3: 165,324,003-165,361,988	LINC01322
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6628003	copy number variation	118	nstd224	human		GRCh37 chr2: 228,241,621-228,258,199 , GRCh38.p12 chr2: 227,376,905-227,393,483	TM4SF20
nsv6621727	copy number variation	5	nstd224	human		GRCh37 chr12: 63,942,707-64,119,228 , GRCh38.p12 chr12: 63,548,927-63,725,448	DPY19L2, LOC100418730, 2 more genes
nsv6629247	copy number variation	65	nstd224	human		GRCh37 chr3: 75,447,252-75,550,939 , GRCh38.p12 chr3: 75,398,101-75,501,788	FAM86DP, LINC02018, 2 more genes
nsv6626369	copy number variation	153	nstd224	human		GRCh37 chr1: 25,604,951-25,655,563 , GRCh38.p12 chr1: 25,278,460-25,329,072	RSRP1, RHD, 1 more genes
nsv6625675	copy number variation	2	nstd224	human		GRCh37 chr1: 17,211,616-17,260,022 , GRCh38.p12 chr1: 16,885,121-16,933,527	TRN-GTT4-1, RNU1-2, 3 more genes
nsv6628220	copy number variation	1	nstd224	human		GRCh37 chr2: 82,067,949-82,404,967 , GRCh38.p12 chr2: 81,840,825-82,177,843	LOC105374829, LOC102724542, 1 more genes
nsv6624743	copy number variation	35	nstd224	human		GRCh37 chr19: 43,304,337-43,537,972 , GRCh38.p12 chr19: 42,800,185-43,033,820	CEACAMP7, PSG1, 5 more genes
nsv6621453	copy number variation	1	nstd224	human		GRCh37 chr12: 29,943,923-30,016,456 , GRCh38.p12 chr12: 29,790,990-29,863,523	0
nsv6622002	copy number variation	111	nstd224	human		GRCh37 chr14: 20,198,662-20,417,653 , GRCh38.p12 chr14: 19,730,503-19,949,494	OR4N1P, OR4K3, 11 more genes

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OSC6390 AND nstd224 (12)
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