157170 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
nsv4368029	copy number variation	55	nstd173	human		GRCh37 chr10: 68,077,579-68,122,519 , GRCh38.p12 chr10: 66,317,821-66,362,761	CTNNA3
nsv4376754	copy number variation	1	nstd173	human		GRCh37 chr4: 76,962,263-77,004,094 , GRCh38.p12 chr4: 76,041,110-76,082,941	ART3
nsv4384250	copy number variation	1	nstd173	human		GRCh37 chr20: 39,876,086-39,907,054 , GRCh38.p12 chr20: 41,247,446-41,278,414	ZHX3
nsv4371674	copy number variation	102	nstd173	human		GRCh37 chr3: 89,394,610-89,419,375 , GRCh38.p12 chr3: 89,345,460-89,370,225	EPHA3
nsv4377805	copy number variation	1	nstd173	human		GRCh37 chr1: 144,833,673-144,922,878 , GRCh38.p12 chr1: 148,961,597-149,050,768	PDE4DIP
nsv4376823	copy number variation	1	nstd173	human		GRCh37 chr12: 64,689,786-64,720,131 , GRCh38.p12 chr12: 64,296,006-64,326,351	C12orf56
nsv4370116	copy number variation	174	nstd173	human		GRCh37 chr2: 98,138,417-98,161,960 , GRCh38.p12 chr2: 97,521,954-97,545,497	ANKRD36B
nsv4377240	copy number variation	21	nstd173	human		GRCh37 chr8: 39,226,336-39,386,964 , GRCh38.p12 chr8: 39,368,817-39,529,445	ADAM5, ADAM3A
nsv4369336	copy number variation	4	nstd173	human		GRCh37 chr6: 257,065-302,184 , GRCh38.p12 chr6: 257,065-302,184	, DUSP22, 1 more genes
nsv4387832	copy number variation	38	nstd173	human		GRCh37 chr12: 11,216,817-11,256,413 , GRCh38.p12 chr12: 11,064,218-11,103,814	TAS2R43, PRH1-TAS2R14, 3 more genes
nsv4384114	copy number variation	32	nstd173	human		GRCh37 chr17: 44,187,492-44,288,442 , GRCh38.p12 chr17: 46,110,126-46,211,076 , GRCh38.p12 chr17\|NT_187663.1: 812,225-913,250	KANSL1-AS1, LOC107985027, 1 more genes
nsv4369028	copy number variation	48	nstd173	human		GRCh37 chr17: 34,439,965-34,477,480 , GRCh38.p12 chr17: 36,112,572-36,150,098 , GRCh38.p12 chr17\|NT_187661.1: 66,669-104,195 , GRCh38.p12 chr17\|NT_187614.1: 347,493-385,008	, LOC100419980, 2 more genes
nsv4373540	copy number variation	34	nstd173	human		GRCh37 chr19: 20,598,430-20,720,705 , GRCh38.p12 chr19: 20,415,624-20,537,899	ZNF826P, ZNF737, 4 more genes
nsv4382973	copy number variation	317	nstd173	human		GRCh37 chr5: 180,378,754-180,442,428 , GRCh38.p12 chr5: 180,951,754-181,015,428	BTNL3, LOC100128762, 4 more genes
nsv4372173	copy number variation	1	nstd173	human		GRCh37 chr1: 145,289,812-145,932,455 , GRCh38.p12 chr1: 145,601,946-146,148,364	RNVU1-6, LIX1L-AS1, 27 more genes

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