wnt16[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3894074	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 120,864,414-121,086,762 , GRCh38.p12 chr7: 121,224,360-121,446,708	WNT16, CPED1, 3 more genes
nsv3923564	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 120,594,858-120,831,965 , GRCh37.p13 chr7: 120,807,622-121,044,729 , GRCh38.p12 chr7: 121,167,568-121,404,675	WNT16, FAM3C, 3 more genes
nsv6290807	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 120,813,156-121,033,289 , GRCh38.p12 chr7: 121,173,102-121,393,235	WNT16, FAM3C, 2 more genes
nsv4456742	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 120,818,380-121,033,193 , GRCh38.p12 chr7: 121,178,326-121,393,139	WNT16, RNU6-517P, 2 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	WNT16, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	WNT16, LOC107986817, 2014 more genes
nsv3916726	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 116,754,095-134,125,980 , GRCh38 chr7: 117,326,805-134,790,689 , GRCh37 chr7: 116,966,859-134,475,440	WNT16, LOC107986845, 245 more genes
nsv4675322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860	WNT16, CBLL1-AS1, 168 more genes
nsv3900620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,613,396-127,897,316 , GRCh38.p12 chr7: 111,973,341-128,257,263	WNT16, LSM8, 170 more genes
nsv3923570	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527	WNT16, ANKRD7, 142 more genes
nsv3916529	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 113,782,532-125,480,435 , NCBI36 chr7: 113,569,768-125,267,671 , GRCh38 chr7: 114,142,477-125,840,381	WNT16, CAPZA2, 124 more genes
nsv3922792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 113,227,126-124,326,508 , GRCh37 chr7: 113,439,890-124,539,272 , GRCh38 chr7: 113,799,835-124,899,218	WNT16, MTND4P6, 116 more genes
nsv5381759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640	WNT16, TMEM229A, 110 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	WNT16, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	WNT16, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	WNT16, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	WNT16, TRGV3, 2682 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	WNT16, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	WNT16, CYP3A5, 1144 more genes
nsv4675620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017	WNT16, RPL26P23, 887 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 26

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Number of Variants: 20

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Search details

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