5-0126-001 AND nstd173 - dbVar - NCBI

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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
nsv4372152	copy number variation	236	nstd173	human		GRCh37 chr6: 78,969,092-79,035,184 , GRCh38.p12 chr6: 78,259,375-78,325,467	LOC105377865
nsv4365926	copy number variation	7	nstd173	human		GRCh37 chr20: 1,560,549-1,593,892 , GRCh38.p12 chr20: 1,579,903-1,613,246	SIRPB1
nsv4366800	copy number variation	1	nstd173	human		GRCh37 chr8: 16,262,318-16,294,035 , GRCh38.p12 chr8: 16,404,809-16,436,526	LOC101929028
nsv4372655	copy number variation	1	nstd173	human		GRCh37 chr10: 25,636,901-25,667,609 , GRCh38.p12 chr10: 25,347,972-25,378,680	GPR158
nsv4386429	copy number variation	124	nstd173	human		GRCh37 chr13: 57,758,276-57,778,379 , GRCh38.p12 chr13: 57,184,142-57,204,245	MTCO2P3
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
nsv4379956	copy number variation	132	nstd173	human		GRCh37 chr17: 44,212,824-44,292,754 , GRCh38.p12 chr17: 46,135,458-46,215,388 , GRCh38.p12 chr17\|NT_187663.1: 837,565-917,561	LOC107985027, KANSL1, 1 more genes
nsv4382288	copy number variation	3	nstd173	human		GRCh37 chr11: 89,474,818-89,550,211 , GRCh38.p12 chr11: 89,741,650-89,817,043	UBTFL2, TRIM49, 2 more genes
nsv4384776	copy number variation	87	nstd173	human		GRCh37 chr19: 52,131,800-52,154,905 , GRCh38.p12 chr19: 51,628,547-51,651,652	SIGLEC5, SIGLEC14, 1 more genes
nsv4380276	copy number variation	3	nstd173	human		GRCh37 chr8: 102,388,025-102,408,295 , GRCh38.p12 chr8: 101,375,797-101,396,067	LINC02845, RN7SL563P, 1 more genes
nsv4370191	copy number variation	2	nstd173	human		GRCh37 chrX: 148,884,135-149,089,325 , GRCh38.p12 chrX: 149,802,473-149,921,107	LINC00850, MAGEA8, 3 more genes
nsv4374155	copy number variation	3	nstd173	human		GRCh37 chr10: 48,117,190-48,174,779 , GRCh38.p12 chr10: 47,564,583-47,622,172	LINC02675, ANXA8, 3 more genes
nsv4386828	copy number variation	67	nstd173	human		GRCh37 chr19: 20,596,118-20,716,388 , GRCh38.p12 chr19: 20,413,312-20,533,582	ZNF826P, ZNF737, 4 more genes
nsv4376307	copy number variation	1	nstd173	human		GRCh37 chr15: 23,286,572-23,670,903 , GRCh38.p12 chr15: 22,358,243-22,586,524	LOC112268161, LOC441711, 8 more genes
nsv4368660	copy number variation	868	nstd173	human		GRCh37 chr6: 103,738,197-103,759,824 , GRCh38.p12 chr6: 103,290,322-103,311,949	0
nsv4369274	copy number variation	262	nstd173	human		GRCh37 chr2: 35,976,209-35,997,473 , GRCh38.p12 chr2: 35,751,143-35,772,407	0
nsv4387573	copy number variation	172	nstd173	human		GRCh37 chr11: 54,701,632-54,757,928 , GRCh38.p12 chr11: 54,934,156-54,990,452	0
nsv4377396	copy number variation	94	nstd173	human		GRCh37 chr14: 106,536,991-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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