syngap1[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
nsv6312477	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 33,393,555-33,393,700 , GRCh38.p12 chr6: 33,425,778-33,425,923	SYNGAP1
nsv4682350	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 33,388,022-33,419,703 , GRCh38.p12 chr6: 33,420,245-33,451,926	SYNGAP1, MIR5004
nsv4682695	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 33,402,909-33,406,088 , GRCh38.p12 chr6: 33,435,132-33,438,311	SYNGAP1, MIR5004
nsv997225	copy number variation	1	nstd45	human	Pathogenic	GRCh38.p12 chr6: 33,420,070-33,453,689 , GRCh37 chr6: 33,387,847-33,421,466	SYNGAP1, ZBTB9, 1 more genes
nsv4456439	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,388,971-33,428,369 , GRCh38.p12 chr6: 33,421,194-33,460,592	SYNGAP1, MIR5004, 1 more genes
nsv3913446	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 33,491,109-33,508,684 , GRCh38 chr6: 33,415,354-33,432,929 , GRCh37 chr6: 33,383,131-33,400,706	SYNGAP1, CUTA, 1 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	SYNGAP1, 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	SYNGAP1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SYNGAP1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	SYNGAP1, ITPR3, 2905 more genes
nsv4350067	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 29,455,465-81,447,367 , GRCh38.p12 chr6: 29,487,688-80,737,650	SYNGAP1, HLA-DPB2, 1001 more genes
nsv3913920	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 156,974-46,789,291 , NCBI36 chr6: 101,974-46,864,987 , GRCh37 chr6: 156,974-46,757,028	SYNGAP1, TRR-ACG1-2, 1385 more genes
nsv4768386	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38.p12 chr6: 33,375,382-33,468,170 , NCBI36 chr6: 33,451,137-33,543,925 , GRCh37.p13 chr6: 33,343,159-33,435,947 , GRCh37.p13 chr6\|NT_167249.1: 4,836,050-4,916,187 , GRCh38.p12 chr6\|NT_167249.2: 4,836,753-4,916,889	SYNGAP1, KIFC1, 6 more genes
nsv4675941	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr6: 31,036,397-34,088,832 , GRCh38.p12 chr6: 31,068,620-34,121,055	SYNGAP1, AGER, 217 more genes
nsv7097426	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173	SYNGAP1, LEMD2, 321 more genes
nsv7098787	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 32,148,920-36,953,949 , GRCh38.p12 chr6: 32,181,143-36,986,173	SYNGAP1, CUTA, 184 more genes
nsv6313582	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,069,892-33,751,391 , GRCh38.p12 chr6: 33,102,115-33,783,614	SYNGAP1, LOC107986537, 46 more genes
nsv4451881	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,131,435-33,419,703 , GRCh38 chr6: 33,163,658-33,451,926	SYNGAP1, COL11A2, 29 more genes
nsv4683878	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,359,763-33,640,005 , GRCh38.p12 chr6: 33,391,986-33,672,228	SYNGAP1, ITPR3-AS1, 12 more genes
nsv4682849	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 33,141,458-33,419,703 , GRCh38.p12 chr6: 33,173,681-33,451,926	SYNGAP1, RPL35AP4, 29 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 21

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Number of Variants: 20

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