1-0775-003 AND nstd173 - dbVar - NCBI

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Items: 18

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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
nsv4366725	copy number variation	1	nstd173	human		GRCh37 chr11: 134,355,933-134,477,387 , GRCh38.p12 chr11: 134,486,039-134,607,493	B3GAT1-DT
nsv4373337	copy number variation	44	nstd173	human		GRCh37 chr2: 98,063,359-98,162,176 , GRCh38.p12 chr2: 97,490,656-97,545,713	ANKRD36B
nsv4377994	copy number variation	31	nstd173	human		GRCh37 chr1: 72,773,260-72,811,084 , GRCh38.p12 chr1: 72,307,577-72,345,401 , GRCh38.p12 chr1\|NW_018654707.1: 19,844-66,626	LOC105378797
nsv4379109	copy number variation	1337	nstd173	human		GRCh37 chr20: 1,560,774-1,597,997 , GRCh38.p12 chr20: 1,580,128-1,617,351	SIRPB1
nsv4370761	copy number variation	67	nstd173	human		GRCh37 chr16: 55,796,388-55,822,431 , GRCh38.p12 chr16: 55,762,476-55,788,519	CES1P1
nsv4366675	copy number variation	2	nstd173	human		GRCh37 chrX: 81,182,971-81,321,054 , GRCh38.p12 chrX: 81,927,472-82,065,605	RNU6-974P
nsv4385909	copy number variation	6	nstd173	human		GRCh37 chr16: 55,822,788-55,868,426 , GRCh38.p12 chr16: 55,788,876-55,834,514 , GRCh38.p12 chr16\|NW_003315945.1: 22,523-58,419	CES1
nsv4375408	copy number variation	4	nstd173	human		GRCh37 chr8: 39,246,760-39,386,964 , GRCh38.p12 chr8: 39,389,241-39,529,445	ADAM3A, ADAM5
nsv4375714	copy number variation	376	nstd173	human		GRCh37 chr4: 69,435,889-69,485,978 , GRCh38.p12 chr4: 68,570,171-68,620,260	UGT2B17, LOC100132651, 1 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
nsv4367949	copy number variation	1	nstd173	human		GRCh37 chrX: 84,990,565-85,169,681 , GRCh38.p12 chrX: 85,735,560-85,914,676	MIR361, MIR1321, 2 more genes
nsv4379635	copy number variation	108	nstd173	human		GRCh37 chr11: 55,374,019-55,452,996 , GRCh38.p12 chr11: 55,606,543-55,685,520	OR4P4, OR4V1P, 3 more genes
nsv4370277	copy number variation	687	nstd173	human		GRCh37 chr5: 180,378,754-180,430,789 , GRCh38.p12 chr5: 180,951,754-181,003,789	BTNL8, ARPP19P1, 3 more genes
nsv4379003	copy number variation	3	nstd173	human		GRCh37 chr6: 257,061-294,273 , GRCh38.p12 chr6: 257,061-294,273	DUSP22, , 1 more genes
nsv4379692	copy number variation	13	nstd173	human		GRCh37 chr22: 42,514,890-42,540,108 , GRCh38.p12 chr22\|NT_187682.1: 44,856-66,447	CYP2D7, CYP2D6, 4 more genes
nsv4379930	copy number variation	14	nstd173	human		GRCh37 chr14: 22,643,684-22,959,555 , GRCh38.p12 chr14: 22,175,787-22,490,567	TRDJ1, TRD-AS1, 41 more genes
nsv4387566	copy number variation	315	nstd173	human		GRCh37 chr2: 34,701,655-34,727,784 , GRCh38.p12 chr2: 34,476,588-34,502,717	0
nsv4388385	copy number variation	148	nstd173	human		GRCh37 chr14: 106,537,003-106,560,975 , GRCh38.p12 chr: NaN-NaN	0

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