rnasek[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
nsv3913013	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055	RNASEK, RPS4XP17, 289 more genes
nsv3923152	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 3,451,558-7,022,067 , GRCh38 chr17: 3,601,515-7,178,024 , GRCh37 chr17: 3,504,809-7,081,343	RNASEK, PSMB6, 133 more genes
nsv3910343	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 5,636,297-7,942,140 , NCBI36 chr17: 5,577,021-7,882,865 , GRCh38 chr17: 5,732,977-8,038,822	RNASEK, RPL23AP73, 106 more genes
nsv1397967	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 6,838,295-7,991,364 , GRCh37.p13 chr17: 6,897,571-8,050,639 , GRCh38.p12 chr17: 6,994,252-8,147,321	RNASEK, TNFSF12-TNFSF13, 96 more genes
nsv5673052	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117	RNASEK, RPL23AP73, 25 more genes
nsv4676022	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 6,800,893-7,304,696 , GRCh38.p12 chr17: 6,897,574-7,401,377	RNASEK, DVL2, 37 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	RNASEK, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	RNASEK, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	RNASEK, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	RNASEK, SMURF2, 2366 more genes
nsv3897625	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420	RNASEK, GP1BA, 439 more genes
nsv3915354	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519	RNASEK, KIF1C-AS1, 433 more genes
nsv3917059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901	RNASEK, PSMB6, 409 more genes
nsv7148254	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413	RNASEK, RFLNB, 401 more genes
nsv3904771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115	RNASEK, SLC2A4, 401 more genes
nsv3917777	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 50,690-7,394,448 , GRCh38 chr17: 198,748-7,491,129 , NCBI36 chr17: 48,539-7,335,172	RNASEK, PAFAH1B1, 267 more genes
nsv3911050	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391	RNASEK, C17orf49, 209 more genes
nsv4729929	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 6,650,649-8,040,151 , GRCh38.p12 chr17: 6,747,330-8,136,833	RNASEK, CYB5D1, 98 more genes
nsv3911018	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr17: 6,205,437-7,594,906 , GRCh37 chr17: 6,264,713-7,654,181 , GRCh38 chr17: 6,361,393-7,750,863	RNASEK, ACADVL, 87 more genes
nsv1398120	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr17: 6,853,665-8,107,394 , GRCh37.p13 chr17: 6,912,941-8,166,669 , GRCh38.p12 chr17: 7,009,622-8,263,351	RNASEK, ACADVL, 117 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 26

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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