wnt3[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 16

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Number of Variants: 16

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3893743	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,848,438-44,865,439 , GRCh38.p12 chr17\|NT_167251.2: 1,756,951-1,773,959 , GRCh38.p12 chr17: 46,771,072-46,788,073 , GRCh38.p12 chr17\|NT_187663.1: 1,290,484-1,307,484	WNT3, LRRC37A2
nsv3906300	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,843,136-44,859,143 , GRCh38.p12 chr17\|NT_187663.1: 1,285,183-1,301,190 , GRCh38.p12 chr17\|NT_167251.2: 1,751,649-1,767,663 , GRCh38.p12 chr17: 46,765,770-46,781,777	WNT3, LRRC37A2
nsv6310389	copy number variation	2	nstd102	human	Uncertain significance, Pathogenic	GRCh37 chr17: 44,845,686-45,016,126 , GRCh38.p12 chr17: 46,768,320-46,938,760 , GRCh38.p12 chr17\|NT_187663.1: 1,287,733-1,423,190	WNT3, WNT9B, 6 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	WNT3, PRPSAP1, 1350 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	WNT3, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	WNT3, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	WNT3, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	WNT3, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	WNT3, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	WNT3, FOXK2, 958 more genes
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	WNT3, RNU6-131P, 1075 more genes
nsv3911563	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214	WNT3, PLEKHH3, 958 more genes
nsv3892018	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,629,166-44,870,255 , GRCh38.p12 chr17: 46,551,800-46,792,889 , GRCh38.p12 chr17\|NT_187663.1: 1,071,509-1,312,306 , GRCh38.p12 chr17\|NT_167251.2: 1,640,860-1,778,781	WNT3, NSF, 5 more genes
nsv3916246	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,223,908-44,873,614 , NCBI36 chr17: 41,563,662-42,231,947 , GRCh38 chr17: 46,130,519-46,799,417	WNT3, FAM215B, 16 more genes
nsv3906172	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 44,436,494-44,849,188 , GRCh38.p12 chr17\|NT_187663.1: 1,009,112-1,291,229 , GRCh38.p12 chr17: 46,359,128-46,771,822	WNT3, ARL17A, 8 more genes
nsv3921456	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr17: 46,444,520-46,990,403 , GRCh37 chr17: 44,485,771-45,067,769 , NCBI36 chr17: 41,841,187-42,422,768	WNT3, RPRML, 15 more genes

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