dbVar for Gene (Select 87) - 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
nsv7094510	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 68,699,594-70,654,407 , GRCh38.p12 chr14: 68,232,877-70,187,690	RN7SL108P, SNORD169, 38 more genes
nsv7075321	inversion	1	nstd229	human		GRCh38 chr14: 68,963,930-68,968,228 , GRCh37.p13 chr14: 69,430,647-69,434,945	ACTN1
nsv7068193	inversion	1	nstd229	human		GRCh38 chr14: 65,793,880-70,322,609 , GRCh37.p13 chr14: 66,260,598-70,789,326	BANF1P1, GALNT16-AS1, 78 more genes
nsv7066722	inversion	1	nstd229	human		GRCh38 chr14: 68,945,541-68,945,665 , GRCh37.p13 chr14: 69,412,258-69,412,382	ACTN1
nsv6973734	copy number variation	1	nstd229	human		GRCh38 chr14: 68,938,993-68,948,716 , GRCh37.p13 chr14: 69,405,710-69,415,433	ACTN1
nsv6972222	copy number variation	1	nstd229	human		GRCh38 chr14: 68,969,501-68,973,500 , GRCh37.p13 chr14: 69,436,218-69,440,217	ACTN1
nsv6971350	copy number variation	1	nstd229	human		GRCh38 chr14: 68,929,637-68,929,657 , GRCh37.p13 chr14: 69,396,354-69,396,374	ACTN1
nsv6969110	copy number variation	1	nstd229	human		GRCh38 chr14: 68,922,760-68,927,186 , GRCh37.p13 chr14: 69,389,477-69,393,903	ACTN1
nsv6967145	copy number variation	1	nstd229	human		GRCh38 chr14: 68,951,483-68,951,684 , GRCh37.p13 chr14: 69,418,200-69,418,401	ACTN1
nsv6964967	copy number variation	1	nstd229	human		GRCh38 chr14: 68,959,601-68,961,800 , GRCh37.p13 chr14: 69,426,318-69,428,517	ACTN1
nsv6963906	copy number variation	1	nstd229	human		GRCh38 chr14: 68,871,776-68,874,475 , GRCh37.p13 chr14: 69,338,493-69,341,192	ACTN1
nsv6963221	copy number variation	1	nstd229	human		GRCh38 chr14: 68,942,718-68,954,033 , GRCh37.p13 chr14: 69,409,435-69,420,750	ACTN1
nsv6962257	copy number variation	1	nstd229	human		GRCh38 chr14: 68,964,044-68,968,199 , GRCh37.p13 chr14: 69,430,761-69,434,916	ACTN1
nsv6591861	inversion	1	nstd223	human		GRCh38 chr14: 65,793,878-70,322,614 , GRCh37.p13 chr14: 66,260,596-70,789,331	SLC8A3, GALNT16-AS1, 78 more genes
nsv6491702	copy number variation	1	nstd223	human		GRCh38 chr14: 68,922,481-68,922,709 , GRCh37.p13 chr14: 69,389,198-69,389,426	ACTN1
nsv6476063	copy number variation	1	nstd223	human		GRCh38 chr14: 64,354,345-74,200,229 , GRCh37.p13 chr14: 64,821,063-74,666,932	RNU6-240P, COX7A2P1, 196 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	PAPOLA-DT, LOC105378180, 1338 more genes
nsv6237224	insertion	2	nstd214	human		GRCh38 chr14: 68,929,006-68,929,006 , GRCh37.p13 chr14: 69,395,723-69,395,723	ACTN1
nsv6133135	copy number variation	1	nstd213	human		GRCh37 chr14: 68,890,000-70,620,001 , GRCh38.p12 chr14: 68,423,283-70,153,284	SLC8A3, ACTN1-DT, 33 more genes
nsv6129854	insertion	1	nstd186	human		GRCh37 chr14: 69,417,180-69,417,230 , GRCh38.p12 chr14: 68,950,463-68,950,513	ACTN1

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Number of Variants: 20

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Items: 1 to 20 of 266

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Number of Variants: 20

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