dbVar for Gene (Select 2261) - 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
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLIRPP2, STIM2-AS1, 659 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	OR7E84P, FAM193A, 764 more genes
nsv7137196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072	ECM1P2, LOC105378240, 482 more genes
nsv7097251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-1,843,544 , GRCh38.p12 chr4: 499,336-1,841,817	PDE6B, LOC105374339, 44 more genes
nsv7096846	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,795,662-1,795,790 , GRCh38.p12 chr4: 1,793,935-1,794,063	FGFR3
nsv7093291	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr4: 1,804,435-1,804,506 , GRCh37 chr4: 1,806,162-1,806,233	FGFR3
nsv7039441	inversion	1	nstd229	human		GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175	NOP14-AS1, LOC112268460, 34 more genes
nsv6736417	copy number variation	1	nstd229	human		GRCh38 chr4: 1,801,401-1,870,600 , GRCh37.p13 chr4: 1,803,128-1,872,327	RN7SL671P, LETM1, 2 more genes
nsv6731731	copy number variation	1	nstd229	human		GRCh38 chr4: 1,711,801-1,828,000 , GRCh37.p13 chr4: 1,713,528-1,829,727	LOC112268460, FGFR3, 4 more genes
nsv6730554	copy number variation	1	nstd229	human		GRCh38 chr4: 1,286,014-1,845,501 , GRCh37.p13 chr4: 1,279,802-1,847,228	TMEM129, FGFR3, 12 more genes
nsv6723574	copy number variation	1	nstd229	human		GRCh38 chr4: 1,658,306-1,798,037 , GRCh37.p13 chr4: 1,660,033-1,799,764	TACC3, LOC112268460, 4 more genes
nsv6722981	copy number variation	1	nstd229	human		GRCh38 chr4: 1,732,011-1,794,362 , GRCh37.p13 chr4: 1,733,738-1,796,089	FGFR3, LOC112268460, 1 more genes
nsv6722837	copy number variation	1	nstd229	human		GRCh38 chr4: 1,717,816-1,803,185 , GRCh37.p13 chr4: 1,719,543-1,804,912	TACC3, FGFR3, 2 more genes
nsv6721192	copy number variation	1	nstd229	human		GRCh38 chr4: 1,800,047-1,811,594 , GRCh37.p13 chr4: 1,801,774-1,813,321	LETM1, FGFR3
nsv6720770	copy number variation	1	nstd229	human		GRCh38 chr4: 1,808,240-1,861,252 , GRCh37.p13 chr4: 1,809,967-1,862,979	LETM1, FGFR3
nsv6636691	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-2,437,290 , GRCh38.p12 chr4: 68,454-2,435,563	SPON2, TACC3, 77 more genes
nsv6636582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359	NELFA, OR7E111FP, 289 more genes
nsv6636548	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,734,046-1,871,531 , GRCh38.p12 chr4: 1,732,319-1,869,804	NSD2, TACC3, 4 more genes
nsv6636534	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 963,688-2,913,553 , GRCh38.p12 chr4: 969,900-2,911,826	ADD1, CTBP1, 53 more genes
nsv6636307	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,180,181-2,009,278 , GRCh38.p12 chr4: 1,186,393-2,007,551	LOC105374348, SPON2, 22 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 419

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Number of Variants: 20

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