ilf2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 14

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Number of Variants: 14

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	ILF2, CRB1, 1608 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	ILF2, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	ILF2, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	ILF2, RNU1-153P, 4887 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	ILF2, LOC101060227, 1608 more genes
nsv3900459	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332	ILF2, HORMAD1, 923 more genes
nsv3877540	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 150,853,044-154,647,786 , GRCh38.p12 chr1: 150,880,568-154,675,310	ILF2, LCE1F, 197 more genes
nsv3899785	copy number variation	2	nstd102	human	Uncertain significance, Benign	NCBI36 chr1: 151,880,217-151,991,490 , GRCh37 chr1: 153,613,593-153,724,866 , GRCh38 chr1: 153,641,117-153,752,390	ILF2, SNAPIN, 7 more genes
nsv3889542	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 153,488,723-153,750,339 , GRCh38.p12 chr1: 153,516,247-153,777,863	ILF2, S100A1, 18 more genes
nsv5381285	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699	ILF2, DCST1, 2428 more genes
nsv6310678	copy number variation	4	nstd102	human	Uncertain significance	GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642	ILF2, PRPF3, 352 more genes
nsv4673972	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 153,061,323-153,904,594 , GRCh38.p12 chr1: 153,088,847-153,932,118	ILF2, S100A15A, 46 more genes
nsv4451737	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 153,321,482-153,835,605 , GRCh38.p12 chr1: 153,349,006-153,863,129	ILF2, S100A7, 33 more genes
nsv3876656	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 153,615,996-153,724,866 , GRCh38.p12 chr1: 153,643,520-153,752,390 , GRCh38.p12 chr1\|NW_003315905.1: 1-69,091	ILF2, INTS3, 8 more genes

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