dbVar for Gene (Select 5310) - 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
nsv6112818	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,144,259-2,165,284 , GRCh38.p12 chr16: 2,094,258-2,115,283	PKD1, MIR6511B1, 1 more genes
nsv6112816	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 14,887,031-16,308,753 , GRCh38.p12 chr16: 14,793,174-16,214,896 , GRCh38.p12 chr16\|NT_187607.1: 326,909-1,872,893	NTAN1, MIR3179-1, 50 more genes
nsv6112799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,089,795-2,185,919 , GRCh38.p12 chr16: 2,039,794-2,135,918	NTHL1, PKD1, 6 more genes
nsv6112797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012	ANTKMT, HBA1, 307 more genes
nsv6112776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,140,783-2,187,415 , GRCh38.p12 chr16: 2,090,782-2,137,414	PKD1, MIR1225, 4 more genes
nsv5980385	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,098,616-2,138,611 , GRCh38.p12 chr16: 2,048,615-2,088,610	MIR1225, PKD1, 1 more genes
nsv5975494	insertion	1	nstd209	human		GRCh38 chr16: 2,104,921-2,104,921 , GRCh37.p13 chr16: 2,154,922-2,154,922	PKD1, MIR6511B1
nsv5939446	copy number variation	1	nstd209	human		GRCh38 chr16: 2,089,303-2,089,359 , GRCh37.p13 chr16: 2,139,304-2,139,360	PKD1, TSC2, 1 more genes
nsv5937777	copy number variation	1	nstd209	human		GRCh38 chr16: 2,091,243-2,091,292 , GRCh37.p13 chr16: 2,141,244-2,141,293	PKD1, PKD1-AS1
nsv5936431	copy number variation	1	nstd209	human		GRCh38 chr16: 2,098,322-2,098,943 , GRCh37.p13 chr16: 2,148,323-2,148,944	PKD1
nsv5931737	copy number variation	1	nstd209	human		GRCh38 chr16: 2,087,923-2,087,990 , GRCh37.p13 chr16: 2,137,924-2,137,991	PKD1, TSC2
nsv5672994	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 2,133,686-2,138,611 , GRCh38.p12 chr16: 2,083,685-2,088,610	PKD1, TSC2, 1 more genes
nsv5672922	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr16: 2,135,165-2,138,160 , GRCh38.p12 chr16: 2,085,164-2,088,159	PKD1, TSC2
nsv5672841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,134,223-2,136,878 , GRCh38.p12 chr16: 2,084,222-2,086,877	TSC2, PKD1
nsv5672839	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,103,323-2,185,710 , GRCh38.p12 chr16: 2,053,322-2,135,709	PKD1, TSC2, 5 more genes
nsv5672753	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr16: 2,182,491-2,188,216 , GRCh38 chr16: 2,132,490-2,138,215	PKD1, MIR3180-5, 1 more genes
nsv5662891	insertion	1	nstd207	human		GRCh38 chr16: 2,104,181-2,104,181 , GRCh37.p13 chr16: 2,154,182-2,154,182	PKD1
nsv5656047	insertion	2	nstd207	human		GRCh38 chr16: 2,104,921-2,104,921 , GRCh37.p13 chr16: 2,154,922-2,154,922	PKD1, MIR6511B1
nsv5653750	insertion	1	nstd207	human		GRCh38 chr16: 2,091,315-2,091,315 , GRCh37.p13 chr16: 2,141,316-2,141,316	PKD1, PKD1-AS1
nsv5653037	insertion	1	nstd207	human		GRCh38 chr16: 2,121,971-2,121,971 , GRCh37.p13 chr16: 2,171,972-2,171,972	PKD1

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Number of Variants: 20

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