lgr5[All Fields] AND 1[has_clinical] - 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
nsv3897010	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 71,886,578-71,889,432 , GRCh38.p12 chr12: 71,492,798-71,495,652	LGR5
nsv3896057	copy number variation	1	nstd102	human	Benign	GRCh37 chr12: 71,736,740-71,863,839 , GRCh38.p12 chr12: 71,342,960-71,470,059	LGR5
nsv3920828	copy number variation	1	nstd102	human	Likely benign	GRCh38 chr12: 71,355,673-71,468,955 , GRCh37 chr12: 71,749,453-71,862,735 , NCBI36 chr12: 70,035,720-70,149,002	LGR5
nsv3912172	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr12: 70,007,148-70,172,681 , GRCh37.p13 chr12: 71,720,881-71,886,414 , GRCh38.p12 chr12: 71,327,101-71,492,634	LGR5
nsv3892030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 69,608,090-89,629,345 , GRCh38.p12 chr12: 69,214,310-89,235,568	LGR5, LOC101928002, 197 more genes
nsv3924329	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 70,731,264-82,154,924 , GRCh38 chr12: 70,337,484-81,761,145 , NCBI36 chr12: 69,017,531-80,679,055	LGR5, NAV3, 118 more genes
nsv6112755	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599	LGR5, LINC02421, 144 more genes
nsv3924723	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 70,163,517-77,357,997 , NCBI36 chr12: 68,449,784-75,882,128 , GRCh38 chr12: 69,769,737-76,964,217	LGR5, KRR1, 80 more genes
nsv6291127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 70,084,476-77,065,764 , GRCh38.p12 chr12: 69,690,696-76,671,984	LGR5, LOC100130268, 78 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	LGR5, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	LGR5, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	LGR5, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	LGR5, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	LGR5, OR5BT1P, 2441 more genes
nsv3918556	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr12: 66,691,464-74,063,101 , GRCh37 chr12: 68,405,197-75,776,834 , GRCh38 chr12: 68,011,417-75,383,054	LGR5, CPM, 97 more genes
nsv3898089	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr12: 70,575,476-73,344,659 , GRCh38.p12 chr12: 70,181,696-72,950,879	LGR5, CNOT2, 25 more genes
nsv4455767	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr12: 71,081,550-73,526,446 , GRCh38.p12 chr12: 70,687,770-73,132,666	LGR5, LOC105369832, 17 more genes

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