79220 AND nstd173 - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4368568	copy number variation	177	nstd173	human		GRCh37 chr14: 41,610,556-41,657,457 , GRCh38.p12 chr14: 41,141,353-41,188,254	LINC02315
nsv4376702	copy number variation	1	nstd173	human		GRCh37 chr3: 41,093,451-41,139,829 , GRCh38.p12 chr3: 41,051,960-41,098,338	LOC105377045
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
nsv4371509	copy number variation	47	nstd173	human		GRCh37 chr10: 124,358,181-124,382,444 , GRCh38.p12 chr10: 122,598,665-122,622,928	DMBT1
nsv4386315	copy number variation	17	nstd173	human		GRCh37 chr1: 248,753,184-248,795,277 , GRCh38.p12 chr1: 248,589,883-248,631,976	OR2T11, OR2T10
nsv4374432	copy number variation	3	nstd173	human		GRCh37 chr1: 9,304,745-9,399,793 , GRCh38.p12 chr1: 9,244,686-9,339,734	H6PD, SPSB1
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
nsv4380451	copy number variation	20	nstd173	human		GRCh37 chr12: 11,215,480-11,251,705 , GRCh38.p12 chr12: 11,062,881-11,099,106	TAS2R64P, TAS2R43, 3 more genes
nsv4379443	copy number variation	53	nstd173	human		GRCh37 chr6: 29,837,158-29,874,629 , GRCh38.p12 chr6: 29,869,381-29,906,852	HLA-H, HLA-T, 4 more genes
nsv4378481	copy number variation	186	nstd173	human		GRCh37 chr2: 4,208,245-4,234,699 , GRCh38.p12 chr2: 4,160,655-4,187,109	0
nsv4368907	copy number variation	1	nstd173	human		GRCh37 chr14: 106,536,991-106,763,647 , GRCh38.p12 chr14: 106,112,755-106,307,388 , GRCh38.p12 chr14\|NT_187600.1: 502,910-1,214,078	IGHV1-69, SLC20A1P2, 113 more genes
nsv4374883	copy number variation	14	nstd173	human		GRCh37 chr17: 44,188,391-44,784,639 , GRCh38.p12 chr17: 46,111,025-46,707,273 , GRCh38.p12 chr17\|NT_187663.1: 813,124-1,226,699	DND1P2, RN7SL656P, 14 more genes
nsv4375229	copy number variation	71	nstd173	human		GRCh37 chr2: 34,701,643-34,723,190 , GRCh38.p12 chr2: 34,476,576-34,498,123	0

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