OSC6529 AND nstd224 - 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
nsv6629898	copy number variation	832	nstd224	human		GRCh37 chr4: 69,401,172-69,435,811 , GRCh38.p12 chr4: 68,535,454-68,570,093	UGT2B17
nsv6625091	copy number variation	291	nstd224	human		GRCh37 chr1: 110,228,505-110,241,385 , GRCh38.p12 chr1: 109,685,883-109,698,763	GSTM1
nsv6633012	copy number variation	2	nstd224	human		GRCh37 chr8: 58,394,190-58,542,880 , GRCh38.p12 chr8: 57,481,631-57,630,321	LOC105375855
nsv6626355	copy number variation	1	nstd224	human		GRCh37 chr1: 246,374,869-246,434,447 , GRCh38.p12 chr1: 246,211,567-246,271,145	SMYD3
nsv6628486	copy number variation	45	nstd224	human		GRCh37 chr3: 173,250,261-173,279,541 , GRCh38.p12 chr3: 173,532,471-173,561,751	NLGN1
nsv6626075	copy number variation	20	nstd224	human		GRCh37 chr1: 196,821,486-196,876,278 , GRCh38.p12 chr1: 196,852,356-196,907,148	CFHR4, LOC100996886
nsv6626120	copy number variation	1	nstd224	human		GRCh37 chr1: 246,099,794-246,280,747 , GRCh38.p12 chr1: 245,936,492-246,117,445	SMYD3-AS1, SMYD3
nsv6629247	copy number variation	65	nstd224	human		GRCh37 chr3: 75,447,252-75,550,939 , GRCh38.p12 chr3: 75,398,101-75,501,788	FAM86DP, LINC02018, 2 more genes
nsv6625565	copy number variation	18	nstd224	human		GRCh37 chr1: 12,865,657-12,921,386 , GRCh38.p12 chr1: 12,805,521-12,861,531 , GRCh38.p12 chr1\|NW_012132914.1: 1-43,044	PRAMEF2, PRAMEF11, 3 more genes
nsv6628024	copy number variation	2	nstd224	human		GRCh37 chr2: 241,623,458-241,689,865 , GRCh38.p12 chr2: 240,684,041-240,750,448	LOC285191, AQP12A, 2 more genes
nsv6627372	copy number variation	20	nstd224	human		GRCh37 chr22: 24,301,973-24,402,531 , GRCh38.p12 chr22\|NT_187633.1: 196,148-296,706	DDTL, MTND1P13, 10 more genes
nsv6627610	copy number variation	2	nstd224	human		GRCh37 chr2: 194,915,066-194,985,769 , GRCh38.p12 chr2: 194,050,342-194,121,045	0
nsv6632672	copy number variation	1	nstd224	human		GRCh37 chr8: 138,091,805-138,104,937 , GRCh38.p12 chr8: 137,079,562-137,092,694	0
nsv6630589	copy number variation	1	nstd224	human		GRCh37 chr5: 21,585,236-21,917,519 , GRCh38.p12 chr5: 21,585,127-21,917,410	CDH12, HSPD1P1, 4 more genes
nsv6630495	copy number variation	1	nstd224	human		GRCh37 chr5: 17,025,201-17,234,908 , GRCh38.p12 chr5: 17,025,092-17,234,799	BASP1, BASP1-AS1, 4 more genes
nsv6625293	copy number variation	1	nstd224	human		GRCh37 chr19: 53,958,126-54,511,915 , GRCh38.p12 chr19: 53,454,872-54,008,661	ZNF331, CACNG7, 82 more genes
nsv6625432	copy number variation	1	nstd224	human		GRCh37 chr19: 55,014,124-55,159,164 , GRCh38.p12 chr19: 54,502,908-54,647,715 , GRCh38.p12 chr19\|NT_187693.1: 485,238-630,278 , GRCh38.p12 chr19\|NW_003571060.1: 407,623-552,594 , GRCh38.p12 chr19\|NW_003571054.1: 409,113-554,099	LOC105372460, LILRB1, 8 more genes

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