M2327 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
nsv3318877	copy number variation	1	nstd157	human		GRCh37 chr7: 36,374,361-36,396,593 , GRCh38.p12 chr7: 36,334,752-36,356,984	MATCAP2
nsv3317653	copy number variation	5	nstd157	human		GRCh37 chr7: 111,943,602-111,960,972 , GRCh38.p12 chr7: 112,303,547-112,320,917	ZNF277
nsv3317836	copy number variation	19	nstd157	human		GRCh37 chr18: 67,208,806-67,217,271 , GRCh38.p12 chr18: 69,541,570-69,550,035	DOK6
nsv3318953	copy number variation	35	nstd157	human		GRCh37 chr3: 53,032,639-53,038,786 , GRCh38.p12 chr3: 52,998,623-53,004,770	SFMBT1
nsv3317771	copy number variation	10	nstd157	human		GRCh37 chr3: 128,382,258-128,412,024 , GRCh38.p12 chr3: 128,663,415-128,693,181	POU5F1P6
nsv3318415	copy number variation	1	nstd157	human		GRCh37 chr1: 146,706,068-146,731,367 , GRCh38.p12 chr1: 147,234,422-147,259,713	CHD1L
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
nsv3317701	copy number variation	1	nstd157	human		GRCh37 chr20: 14,201,022-14,244,857 , GRCh38.p12 chr20: 14,220,376-14,264,211	MACROD2, RN7SL864P
nsv3317277	copy number variation	1	nstd157	human		GRCh38.p12 chr14: 21,573,955-21,608,296 , GRCh37 chr14: 22,042,093-22,076,447	OR10G1P, ACTR3P1
nsv3318683	copy number variation	1	nstd157	human		GRCh38.p12 chr19: 54,225,207-54,233,134 , GRCh37 chr19: 54,729,079-54,737,010 , GRCh38.p12 chr19\|NW_003571060.1: 200,197-208,123 , GRCh38.p12 chr19\|NW_003571054.1: 200,007-207,943 , GRCh38.p12 chr19\|NT_187693.1: 200,193-208,124	LOC100421130, LOC107985279
nsv3318379	copy number variation	4	nstd157	human		GRCh37 chr3: 100,340,145-100,439,759 , GRCh38.p12 chr3: 100,621,301-100,720,915	TFG, ADGRG7, 1 more genes
nsv3317632	copy number variation	6	nstd157	human		GRCh38.p12 chr1: 103,562,368-103,618,605 , GRCh37 chr1: 104,104,990-104,161,227	AMY2A, AMY2B, 1 more genes
nsv3318809	copy number variation	11	nstd157	human		GRCh38.p12 chr10: 133,429,369-133,567,018 , GRCh37 chr10: 135,242,873-135,380,522	CYP2E1, OR7M1P, 7 more genes
nsv3317861	copy number variation	37	nstd157	human		GRCh37 chr6: 67,011,900-67,048,885 , GRCh38.p12 chr6: 66,302,007-66,338,992	0
nsv3317271	copy number variation	1	nstd157	human		GRCh37 chr14: 42,562,622-42,568,527 , GRCh38.p12 chr14: 42,093,419-42,099,324	0
nsv3317244	copy number variation	2	nstd157	human		GRCh38.p12 chr21: 10,661,578-10,731,641 , GRCh37 chr21: 10,780,816-10,850,879	0
nsv3318671	copy number variation	17	nstd157	human		GRCh37 chr5: 180,176,005-180,195,526 , GRCh38.p12 chr5: 180,749,005-180,768,526	0

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M2327 AND nstd157 (18)
dbVar
ZNF804B zinc finger protein 804B [Homo sapiens]
ZNF804B zinc finger protein 804B [Homo sapiens]
Gene ID:219578

Gene
Gene Links for dbVar (Select 47178084) (1)
Gene

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