M2193 AND nstd157 - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3318166	copy number variation	1	nstd157	human		GRCh37 chr7: 145,928,594-146,110,464 , GRCh38.p12 chr7: 146,231,502-146,413,372	CNTNAP2
nsv3317666	copy number variation	21	nstd157	human		GRCh37 chr21: 10,715,343-10,883,039 , GRCh38.p12 chr21: 10,629,418-10,797,114	IGHV1OR21-1
nsv3317736	copy number variation	10	nstd157	human		GRCh38.p12 chr14: 85,991,608-86,022,749 , GRCh37 chr14: 86,457,952-86,489,093	LINC02328, LINC02316
nsv3318924	copy number variation	14	nstd157	human		GRCh38.p12 chr15: 97,271,952-97,288,602 , GRCh37 chr15: 97,815,182-97,831,832	LOC105371006, LINC02253
nsv3317555	copy number variation	1	nstd157	human		GRCh38.p12 chr4: 106,363,410-106,464,872 , GRCh37 chr4: 107,284,567-107,386,029	GIMD1, LINC02173
nsv3318588	copy number variation	20	nstd157	human		GRCh38.p12 chr2: 38,729,805-38,744,481 , GRCh37 chr2: 38,956,947-38,971,623	SRSF7, GALM
nsv3317200	copy number variation	7	nstd157	human		GRCh37 chr17: 44,166,604-44,288,620 , GRCh38.p12 chr17: 46,089,238-46,211,254 , GRCh38.p12 chr17\|NT_187663.1: 791,339-913,427	KANSL1, KANSL1-AS1, 1 more genes
nsv3317327	copy number variation	24	nstd157	human		GRCh38.p12 chr2: 241,911,938-242,092,368 , GRCh37 chr2: 242,854,089-243,034,519 , GRCh38.p12 chr2\|NT_187647.1: 1-136,078 , GRCh38.p12 chr2\|NT_187523.1: 1-136,438	LOC285097, LINC01881, 4 more genes
nsv3318316	copy number variation	72	nstd157	human		GRCh37 chr14: 41,615,868-41,661,685 , GRCh38.p12 chr14: 41,146,665-41,192,482	0
nsv3317095	copy number variation	1	nstd157	human		GRCh37 chr4: 58,760,786-58,791,086 , GRCh38.p12 chr4: 57,894,620-57,924,920	0
nsv3317289	copy number variation	24	nstd157	human		GRCh37 chr9: 24,502,737-24,518,795 , GRCh38.p12 chr9: 24,502,739-24,518,797	0
nsv3317844	copy number variation	7	nstd157	human		GRCh37 chr2: 165,850,456-165,864,123 , GRCh38.p12 chr2: 164,993,946-165,007,613	0
nsv3318498	copy number variation	17	nstd157	human		GRCh37 chr4: 108,064,023-108,076,102 , GRCh38.p12 chr4: 107,142,866-107,154,945	0
nsv3317474	copy number variation	4	nstd157	human		GRCh37 chr15: 86,511,657-86,521,133 , GRCh38.p12 chr15: 85,968,426-85,977,902	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
nsv3318882	copy number variation	1	nstd157	human		GRCh38.p12 chr1: 91,749,532-92,162,209 , GRCh37 chr1: 92,215,089-92,627,766	BRDT, PRKAR1AP1, 7 more genes
nsv3318816	copy number variation	1	nstd157	human		GRCh38.p12 chr10: 41,748,210-41,770,769 , GRCh37 chr10: 42,469,440-42,491,999	0

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