syne1[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
nsv6312562	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,485,278-152,485,480 , GRCh38.p12 chr6: 152,164,143-152,164,345	SYNE1
nsv6312235	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 152,652,198-152,658,654 , GRCh38.p12 chr6: 152,331,063-152,337,519	SYNE1
nsv6312311	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 152,644,544-152,644,693 , GRCh38 chr6: 152,323,409-152,323,558	SYNE1
nsv5674008	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 152,466,612-152,643,033 , GRCh38.p12 chr6: 152,145,477-152,321,898	SYNE1
nsv6312563	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,527,283-152,532,743 , GRCh38.p12 chr6: 152,206,148-152,211,608	SYNE1
nsv7097047	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,599,204-152,603,135 , GRCh38.p12 chr6: 152,278,069-152,282,000	SYNE1
nsv7136995	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 152,861,157-152,957,772 , GRCh38.p12 chr6: 152,540,022-152,636,637	SYNE1, NANOGP11
nsv7097422	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 152,716,631-152,765,733 , GRCh38.p12 chr6: 152,395,496-152,444,598	SYNE1, RNA5SP223
nsv4456216	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,209,421-152,645,055 , GRCh38.p12 chr6: 151,888,286-152,323,920	SYNE1, ESR1
nsv4452614	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,443,551-152,534,914 , GRCh38 chr6: 152,122,416-152,213,779	SYNE1, ESR1
nsv6636550	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,569,070-152,838,129 , GRCh38.p12 chr6: 152,247,935-152,516,994	SYNE1, RNA5SP223, 1 more genes
nsv3902069	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,613,587-152,772,375 , GRCh38.p12 chr6: 152,292,452-152,451,240	SYNE1, RNA5SP223, 1 more genes
nsv4675082	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 152,614,123-152,771,099 , GRCh38.p12 chr6: 152,292,988-152,449,964	SYNE1, SYNE1-AS1, 1 more genes
nsv3916405	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 150,744,068-159,894,974 , GRCh38 chr6: 150,381,239-159,553,952 , GRCh37 chr6: 150,702,375-159,974,984	SYNE1, LOC112267968, 126 more genes
nsv3920651	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499	SYNE1, PPP1R14C, 107 more genes
nsv7148221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 150,905,553-158,511,926 , GRCh37.p13 chr6: 151,226,689-158,932,958	SYNE1, RNU6-824P, 97 more genes
nsv4675234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929	SYNE1, RNU7-3P, 86 more genes
nsv3882645	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 152,443,551-153,748,051 , GRCh38 chr6: 152,122,416-153,426,916	SYNE1, LOC107986661, 18 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	SYNE1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	SYNE1, RNU6-411P, 2910 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 36

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Number of Variants: 20

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