znf277[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
nsv3904081	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 111,932,195-111,992,832 , GRCh38.p12 chr7: 112,292,140-112,352,777	ZNF277
nsv3874797	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 112,315,893-112,320,045 , GRCh37 chr7: 111,955,948-111,960,100	ZNF277
nsv4674870	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 111,642,645-111,873,378 , GRCh38.p12 chr7: 112,002,590-112,233,323	ZNF277, DOCK4
nsv4456629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 111,772,148-111,869,174 , GRCh38.p12 chr7: 112,132,093-112,229,119	ZNF277, DOCK4
nsv3901918	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 111,303,344-111,922,531 , GRCh38.p12 chr7: 111,663,288-112,282,476	ZNF277, DOCK4-AS1, 3 more genes
nsv4675512	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 111,823,490-111,938,673 , GRCh38.p12 chr7: 112,183,435-112,298,618	ZNF277, DOCK4, 1 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	ZNF277, 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	ZNF277, LOC107986817, 2014 more genes
nsv3924380	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 101,912,320-120,918,695 , GRCh38 chr7: 102,196,924-121,278,641 , NCBI36 chr7: 101,626,924-120,705,931	ZNF277, LOC102724434, 222 more genes
nsv6313576	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106	ZNF277, LHFPL3-AS2, 233 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	ZNF277, 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	ZNF277, 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	ZNF277, ANKRD7, 142 more genes
nsv3912378	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 101,807,149-112,414,850 , GRCh37 chr7: 101,450,429-112,054,905 , NCBI36 chr7: 101,237,149-111,842,141	ZNF277, DNAJC2, 139 more genes
nsv4455557	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 107,410,314-117,825,549 , GRCh38.p12 chr7: 107,769,869-118,185,495	ZNF277, RAC1P6, 103 more genes
nsv3877875	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 108,290,244-114,759,023 , GRCh37.p13 chr7: 108,503,008-114,971,787 , GRCh38.p12 chr7: 108,862,564-115,331,733	ZNF277, GPR85, 43 more genes
nsv3891918	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 111,642,645-115,770,275 , GRCh38.p12 chr7: 112,002,590-116,130,221	ZNF277, FOXP2, 33 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	ZNF277, 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	ZNF277, 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	ZNF277, MNX1-AS2, 2682 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 46

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Number of Variants: 20

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Supplemental Content

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