hnf1b[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
nsv4436113	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 36,091,585-36,091,820 , GRCh38 chr17: 37,731,594-37,731,829	HNF1B
nsv4578411	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 37,739,500-37,739,574 , GRCh37 chr17: 36,099,491-36,099,565	HNF1B
nsv4436247	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 36,070,510-36,070,670 , GRCh38 chr17: 37,710,502-37,710,662	HNF1B, LOC105371754
nsv4578361	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 36,070,509-36,070,510 , GRCh38 chr17: 37,710,501-37,710,502	HNF1B, LOC105371754
nsv4436760	delins	1	nstd102	human	Pathogenic	GRCh37 chr17: 36,069,807-36,070,965 , GRCh38 chr17: 37,709,799-37,710,957	HNF1B, LOC105371754
nsv7136941	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 36,046,433-36,105,070 , GRCh38.p12 chr17: 37,686,430-37,745,079 , GRCh38.p12 chr17\|NT_187614.1: 1,925,498-1,984,135	HNF1B, LOC107985009, 2 more genes
nsv4684363	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 36,047,375-36,104,875 , GRCh38.p12 chr17: 37,687,372-37,744,884 , GRCh38.p12 chr17\|NT_187614.1: 1,926,440-1,983,940	HNF1B, LOC105371755, 2 more genes
nsv997073	copy number variation	1	nstd45	human	Pathogenic	GRCh37 chr17: 36,046,434-36,105,069 , GRCh38.p12 chr17: 37,686,431-37,745,078 , GRCh38.p12 chr17\|NT_187614.1: 1,925,499-1,984,134	HNF1B, LOC105371754, 2 more genes
nsv4684347	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr17: 33,133,217-33,318,471 , GRCh37 chr17: 36,059,104-36,244,358 , GRCh38 chr17\|NT_187614.1: 1,938,169-2,123,423	HNF1B, LOC105371754, 3 more genes
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	HNF1B, PRPSAP1, 1350 more genes
nsv1397979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,360,227-36,473,024 , GRCh38.p12 chr17\|NT_187614.1: 267,755-2,352,089	HNF1B, LOC100420852, 68 more genes
nsv6315528	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,463,923-36,410,559 , GRCh38.p12 chr17\|NT_187614.1: 371,451-2,289,624	HNF1B, LOC105371750, 60 more genes
nsv3894286	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,477,385-36,404,555 , GRCh38.p12 chr17\|NT_187614.1: 384,913-2,283,620	HNF1B, SNORA90, 59 more genes
nsv4684299	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,384,281-33,322,972 , GRCh38 chr17\|NT_187614.1: 267,696-2,127,924 , GRCh37 chr17: 34,360,168-36,248,859	HNF1B, DHRS11, 58 more genes
nsv3884569	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,143,765-37,995,300 , GRCh37.p13 chr17: 34,900,240-35,888,667	HNF1B, DUSP14, 54 more genes
nsv3898674	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,447,113-36,283,612 , GRCh38.p12 chr17\|NT_187614.1: 354,641-2,162,677 , GRCh38.p12 chr17: 36,119,723-37,924,067	HNF1B, TBC1D3F, 56 more genes
nsv3907616	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,475,679-36,311,009 , GRCh38.p12 chr17\|NT_187614.1: 383,207-2,190,074	HNF1B, TBC1D3H, 56 more genes
nsv3902415	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,475,679-36,283,612 , GRCh38.p12 chr17: 36,148,298-37,924,067 , GRCh38.p12 chr17\|NT_187614.1: 383,207-2,162,677	HNF1B, LOC105371756, 55 more genes
nsv3916783	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,817,422-36,263,019 , GRCh38 chr17: 36,446,545-38,225,796 , NCBI36 chr17: 31,891,535-33,635,633	HNF1B, ACACA, 50 more genes
nsv3892075	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 34,450,405-36,248,918 , NCBI36 chr17: 31,474,518-33,323,031 , GRCh38.p12 chr17: 36,123,019-37,889,296 , GRCh38.p12 chr17\|NT_187614.1: 357,933-2,127,983	HNF1B, RPL18AP12, 52 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 123

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Number of Variants: 20

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