M2152 AND nstd157 - dbVar - NCBI

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Number of Variants: 13

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3317580	copy number variation	32	nstd157	human		GRCh37 chr7: 156,387,296-156,394,307 , GRCh38.p12 chr7: 156,594,602-156,601,613	RNF32-DT
nsv3318326	copy number variation	1	nstd157	human		GRCh37 chr2: 212,547,041-212,552,307 , GRCh38.p12 chr2: 211,682,316-211,687,582	ERBB4
nsv3318323	copy number variation	11	nstd157	human		GRCh37 chr4: 161,952,228-162,003,624 , GRCh38.p12 chr4: 161,031,076-161,082,472	LOC105377514
nsv3318092	copy number variation	14	nstd157	human		GRCh37 chr2: 228,244,107-228,258,198 , GRCh38.p12 chr2: 227,379,391-227,393,482	TM4SF20
nsv3318495	copy number variation	28	nstd157	human		GRCh37 chr11: 18,949,220-18,961,743 , GRCh38.p12 chr11: 18,927,673-18,940,196	MRGPRX1
nsv3318830	copy number variation	2	nstd157	human		GRCh37 chr3: 113,572,819-113,619,872 , GRCh38.p12 chr3: 113,853,972-113,901,025	GRAMD1C, CTDNEP1P1
nsv3318508	copy number variation	6	nstd157	human		GRCh38.p12 chr1: 1,449,831-1,495,327 , GRCh37 chr1: 1,385,211-1,430,707	ATAD3B, ATAD3C
nsv3318042	copy number variation	23	nstd157	human		GRCh38.p12 chr19: 53,015,494-53,049,043 , GRCh37 chr19: 53,518,747-53,552,296	ERVV-1, ERVV-2
nsv3317981	copy number variation	1	nstd157	human		GRCh38.p12 chr: NaN-NaN , GRCh37 chr1: 146,152,553-147,830,375	0
nsv3318502	copy number variation	31	nstd157	human		GRCh37 chr9: 78,004,378-78,011,616 , GRCh38.p12 chr9: 75,389,462-75,396,700	0
nsv3317521	copy number variation	3	nstd157	human		GRCh37 chr9: 8,009,428-8,015,596 , GRCh38.p12 chr9: 8,009,428-8,015,596	0
nsv3318596	copy number variation	6	nstd157	human		GRCh37 chr15: 24,055,488-24,061,557 , GRCh38.p12 chr15: 23,810,341-23,816,410	0
nsv3317821	copy number variation	1	nstd157	human		GRCh37 chr3: 108,598,853-109,020,122 , GRCh38.p12 chr3: 108,880,006-109,301,275	GUCA1C, MORC1, 6 more genes

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