156892 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
nsv4384091	copy number variation	77	nstd173	human		GRCh37 chr11: 49,710,704-49,746,720 , GRCh38.p12 chr11: 49,689,152-49,725,168 , GRCh38.p12 chr11\|NW_019805495.1: 153,334-179,145	GRM5P1
nsv4379737	copy number variation	349	nstd173	human		GRCh37 chr1: 169,216,099-169,241,765 , GRCh38.p12 chr1: 169,246,861-169,272,527	NME7
nsv4365093	copy number variation	508	nstd173	human		GRCh37 chr13: 57,758,269-57,778,379 , GRCh38.p12 chr13: 57,184,135-57,204,245	MTCO2P3
nsv4382074	copy number variation	18	nstd173	human		GRCh37 chr2: 98,138,419-98,162,176 , GRCh38.p12 chr2: 97,521,956-97,545,713	ANKRD36B
nsv4372865	copy number variation	2	nstd173	human		GRCh37 chr11: 4,970,242-4,991,162 , GRCh38.p12 chr11: 4,949,012-4,969,932	OR51A2
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
nsv4380995	copy number variation	1	nstd173	human		GRCh37 chr21: 21,765,093-21,868,712 , GRCh38.p12 chr21: 20,392,781-20,496,400	KRT18P2, RPS3AP1
nsv4373397	copy number variation	1	nstd173	human		GRCh37 chrX: 134,871,801-134,930,645 , GRCh38.p12 chrX: 135,723,961-135,796,656	CT45A5, MGAT2P1, 3 more genes
nsv4382222	copy number variation	125	nstd173	human		GRCh37 chr1: 248,688,587-248,795,289 , GRCh38.p12 chr1: 248,525,286-248,631,988	OR2AS1P, OR2T34, 4 more genes
nsv4380115	copy number variation	25	nstd173	human		GRCh37 chr6: 29,837,188-29,874,629 , GRCh38.p12 chr6: 29,869,411-29,906,852	HLA-H, HLA-T, 4 more genes
nsv4382162	copy number variation	10	nstd173	human		GRCh37 chr3: 65,185,849-65,218,668 , GRCh38.p12 chr3: 65,200,174-65,232,993	0
nsv4368680	copy number variation	1	nstd173	human		GRCh37 chr12: 38,353,875-38,868,380 , GRCh38.p12 chr12: 37,960,073-38,474,578	ALG10B, TUBB8P5, 7 more genes
nsv4377197	copy number variation	1	nstd173	human		GRCh37 chr1: 155,381,661-155,747,960 , GRCh38.p12 chr1: 155,411,870-155,778,169	MSTO1, LOC100419798, 15 more genes
nsv4367343	copy number variation	3	nstd173	human		GRCh37 chr14: 22,688,402-22,959,555 , GRCh38.p12 chr14: 22,220,503-22,490,567	TRDJ4, TRAJ55, 36 more genes
nsv4385529	copy number variation	179	nstd173	human		GRCh37 chr14: 106,525,299-106,692,891 , GRCh38.p12 chr14: 106,069,054-106,236,281 , GRCh38.p12 chr14\|NT_187600.1: 536,823-704,050	IGHVIII-13-1, IGHV1-18, 19 more genes

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