gtf2i[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
nsv3908878	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 74,099,317-74,145,064 , GRCh38.p12 chr7: 74,684,983-74,730,726	GTF2I, GTF2I-AS1
nsv3918603	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 74,681,589-74,753,865 , GRCh37.p13 chr7: 74,843,653-74,915,929 , GRCh38.p12 chr7: 73,137,896-73,174,784	GTF2IP4, SPDYE10
nsv6289984	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,944,168-74,138,459 , GRCh38.p12 chr7: 74,529,838-74,724,126	GTF2I, GTF2IRD1, 3 more genes
nsv3892103	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 74,016,832-74,133,273 , GRCh38.p12 chr7: 74,602,505-74,718,954	GTF2I, GTF2I-AS1, 1 more genes
nsv3920720	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 73,779,626-73,889,366 , GRCh37.p13 chr7\|NW_003871064.1: 2,256,588-2,365,544 , GRCh37.p13 chr7: 74,141,690-74,251,430 , GRCh38.p12 chr7: 74,727,352-74,836,308	GTF2I, PHB1P15, 3 more genes
nsv3924467	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 73,779,626-73,854,093 , GRCh37.p13 chr7\|NW_003871064.1: 2,256,588-2,331,052 , GRCh37.p13 chr7: 74,141,690-74,216,157 , GRCh38.p12 chr7: 74,727,352-74,801,816	GTF2I, NCF1, 3 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	GTF2I, 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	GTF2I, LOC107986817, 2014 more genes
nsv3917508	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 62,196,742-75,061,986 , GRCh38 chr7: 62,736,364-75,432,710 , NCBI36 chr7: 61,834,177-74,899,922	GTF2I, GTF2IP4, 285 more genes
nsv3918722	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909	GTF2I, GTF2IP1, 184 more genes
nsv3922762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112	GTF2I, PMS2P3, 142 more genes
nsv3911276	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 69,382,353-77,823,832 , GRCh37 chr7: 68,847,339-77,453,149 , NCBI36 chr7: 68,485,275-77,291,085	GTF2I, POM121, 155 more genes
nsv3917211	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058	GTF2I, HSPB1, 123 more genes
nsv3914569	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 68,668,307-73,710,276 , NCBI36 chr7: 67,771,230-72,762,542 , GRCh37 chr7: 68,133,294-72,806,397	SPDYE7P, LOC100967223, 61 more genes
nsv4729646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 68,977,230-73,939,510 , GRCh38.p12 chr7: 69,512,244-74,525,180	LOC105375346, ABHD11-AS1, 70 more genes
nsv4728820	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,403,117-76,709,600 , GRCh38.p12 chr7: 72,932,579-77,080,283	GTF2I, FDPSP7, 119 more genes
nsv3902539	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,456,604-76,007,380 , GRCh38.p12 chr7: 72,986,074-76,378,063	GTF2I, WBSCR23, 97 more genes
nsv3922160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 72,404,249-76,189,514 , GRCh38 chr7: 73,352,304-76,722,261 , GRCh37 chr7: 72,766,313-76,351,578	GTF2I, PMS2P10, 88 more genes
nsv4675200	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,621,722-76,007,380 , GRCh38.p12 chr7: 73,207,682-76,378,063	GTF2I, PHB1P15, 87 more genes
nsv4349368	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 72,744,494-76,038,818 , GRCh38.p12 chr7: 73,330,491-76,409,501	GTF2I, MDH2, 83 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 169

Page of 9

Number of Variants: 20

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Find related data

Search details

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