syn3[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
nsv3902923	copy number variation	1	nstd102	human	Benign	GRCh37 chr22: 32,927,211-32,928,401 , GRCh38.p12 chr22: 32,531,224-32,532,414	SYN3
nsv6637628	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,101,137-33,191,344 , GRCh38.p12 chr22: 32,705,151-32,795,358	SYN3
nsv3922536	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr22: 32,940,883-33,084,286 , NCBI36 chr22: 31,666,868-31,810,272 , GRCh37 chr22: 33,336,868-33,480,272	SYN3
nsv4457471	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,067,984-33,370,145 , GRCh38.p12 chr22: 32,671,998-32,974,160	SYN3, TIMP3
nsv3904013	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,209,740-33,403,536 , GRCh38.p12 chr22: 32,813,754-33,007,551	SYN3, TIMP3
nsv5381318	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr22: 33,197,988-33,198,128 , GRCh38.p12 chr22: 32,802,002-32,802,142	SYN3, TIMP3
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	SYN3, LOC100419811, 1084 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	SYN3, IGKV3OR22-2, 1084 more genes
nsv3890411	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035	SYN3, RNU6-495P, 1084 more genes
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	SYN3, FBXO7, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	SYN3, FABP5P11, 1084 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	SYN3, DDTL, 1084 more genes
nsv3890401	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300	SYN3, YPEL1, 1083 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	SYN3, IGLV3-27, 1082 more genes
nsv3891895	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410	SYN3, POM121L7P, 1082 more genes
nsv3913775	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264	SYN3, ZNF280A, 1059 more genes
nsv3919881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079	SYN3, MIR12114, 1059 more genes
nsv3919085	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138	SYN3, IGLV2-28, 1023 more genes
nsv4676292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410	SYN3, PDXP-DT, 550 more genes
nsv3914617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,261,514-37,583,387 , GRCh38 chr22: 20,907,226-37,187,347 , NCBI36 chr22: 19,591,514-35,913,333	SYN3, RASL10A, 525 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 27

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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