gbp7[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 9

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6313574	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 68,180,293-92,731,957 , GRCh38.p12 chr1: 67,714,610-92,266,400	GBP7, RNA5SP51, 315 more genes
nsv3885743	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 72,044,544-92,505,091 , GRCh38.p12 chr1: 71,578,861-92,039,534	GBP7, ZNHIT6, 257 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	GBP7, 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	GBP7, 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	GBP7, 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	GBP7, LINC01773, 322 more genes
nsv4451609	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 89,546,802-90,520,362 , GRCh38.p12 chr1: 89,081,119-90,054,804	GBP7, GBP2, 25 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	GBP7, LINC01776, 1853 more genes
nsv4452508	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 89,239,549-89,733,747 , GRCh38.p12 chr1: 88,773,866-89,268,064	GBP7, LOC107985076, 17 more genes

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gbp7[All Fields] AND 1[has_clinical] (10)
dbVar
3.1.6.3[EC/RN Number] (0)
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