gfi1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv5381077	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 92,941,566-92,949,064 , GRCh38.p12 chr1: 92,476,009-92,483,507	GFI1
nsv3885734	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 92,751,767-92,958,556 , GRCh38.p12 chr1: 92,286,210-92,492,999	GFI1, RN7SL824P, 2 more genes
nsv4768351	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 92,405,898-94,018,197 , GRCh38.p12 chr1: 91,940,341-93,552,640	GFI1, MND1P1, 39 more genes
nsv6313881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 92,626,657-93,345,442 , GRCh38.p12 chr1: 92,161,100-92,879,885	GFI1, LOC100419803, 16 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	GFI1, 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	GFI1, 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	GFI1, RNU1-153P, 4887 more genes
nsv3898327	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 83,457,325-104,273,917 , GRCh37 chr1: 83,923,008-104,816,539 , NCBI36 chr1: 83,695,596-104,618,062	GFI1, LINC01773, 322 more genes
nsv7095872	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 92,941,586-93,307,422 , GRCh38.p12 chr1: 92,476,029-92,841,865	GFI1, SNORD21, 9 more genes
nsv3911827	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr1: 92,600,531-92,884,010 , GRCh37.p13 chr1: 92,827,943-93,111,422 , GRCh38.p12 chr1: 92,362,386-92,645,865	GFI1, HMGB3P9, 5 more genes
nsv4436181	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532	GFI1, LINC01776, 1853 more genes
nsv3873752	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 91,668,330-93,539,185 , GRCh38.p12 chr1: 91,202,773-93,073,628	GFI1, RNU4-59P, 38 more genes

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