syt2[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
nsv3887237	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 202,595,153-202,721,148 , GRCh38.p12 chr1: 202,626,025-202,752,020	SYT2, KDM5B
nsv3908834	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 158,618,491-158,720,799 , GRCh38.p12 chr7: 158,825,800-158,928,108	DYNC2I1, ESYT2
nsv3883570	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37.p13 chr7: 158,519,118-158,986,159 , GRCh38 chr7: 158,726,427-159,193,469	VIPR2, DYNC2I1, 2 more genes
nsv3921987	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr7: 158,587,980-159,119,707 , NCBI36 chr7: 158,280,741-158,812,468 , GRCh38 chr7: 158,795,289-159,327,017	ESYT2, VIPR2, 3 more genes
nsv3903639	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 158,389,294-158,785,846 , GRCh38.p12 chr7: 158,596,602-158,993,155	ESYT2, NCAPG2, 3 more genes
nsv3901177	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 158,584,933-158,962,061 , GRCh38.p12 chr7: 158,792,242-159,169,370	VIPR2, LINC00689, 2 more genes
nsv3873477	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 202,407,113-202,727,279 , GRCh38.p12 chr1: 202,437,985-202,758,151	SYT2, RPS27P8, 3 more genes
nsv6291089	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,397,361-158,630,131 , GRCh38.p12 chr7: 158,604,669-158,837,440	DYNC2I1, ESYT2, 3 more genes
nsv7148260	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr1: 202,434,559-202,604,719 , GRCh37.p13 chr1: 202,403,687-202,573,847	SYT2, PPP1R12B, 2 more genes
nsv3917120	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 158,263,899-158,818,289 , GRCh37.p13 chr7: 158,571,138-159,125,528 , GRCh38.p12 chr7: 158,778,447-159,332,838	PIP5K1P2, ESYT2, 3 more genes
nsv4456589	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,587,979-159,119,707 , GRCh38.p12 chr7: 158,795,288-159,327,017	PIP5K1P2, ESYT2, 3 more genes
nsv4349377	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,587,980-159,119,707 , GRCh38.p12 chr7: 158,795,289-159,327,017	VIPR2, LINC00689, 3 more genes
nsv6636211	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,587,981-159,119,707 , GRCh38.p12 chr7: 158,795,290-159,327,017	VIPR2, PIP5K1P2, 3 more genes
nsv3914989	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 158,238,447-158,735,302 , GRCh37.p13 chr7: 158,545,686-159,042,541 , GRCh38.p12 chr7: 158,752,995-159,249,851	PIP5K1P2, DYNC2I1, 3 more genes
nsv6637096	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,385,219-158,727,591 , GRCh38.p12 chr7: 158,592,527-158,934,900	DYNC2I1, RPL21P76, 3 more genes
nsv3892553	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,393,513-158,727,591 , GRCh38.p12 chr7: 158,600,821-158,934,900	RPL21P76, THAP5P1, 3 more genes
nsv3916252	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 158,178,330-158,494,394 , GRCh37.p13 chr7: 158,485,569-158,801,633 , GRCh38.p12 chr7: 158,692,877-159,008,942	DYNC2I1, LINC00689, 3 more genes
nsv3895374	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,424,788-158,668,137 , GRCh38.p12 chr7: 158,632,096-158,875,446	DYNC2I1, ESYT2, 2 more genes
nsv7099014	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr7: 158,815,519-159,037,266 , GRCh37.p13 chr7: 158,608,210-158,829,957	LINC00689, ESYT2, 2 more genes
nsv4455542	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 158,462,108-158,562,397 , GRCh38.p12 chr7: 158,669,416-158,769,706	ESYT2, NCAPG2, 1 more genes

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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 146

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Number of Variants: 20

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