snapc1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv4456340	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr14: 62,175,968-62,227,772 , GRCh38.p12 chr14: 61,709,250-61,761,054	SNAPC1, HIF1A-AS2, 2 more genes
nsv3922652	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 57,507,754-67,674,948 , NCBI36 chr14: 56,577,507-66,744,701 , GRCh38 chr14: 57,041,036-67,208,231	SNAPC1, PARP1P2, 160 more genes
nsv3923965	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 60,383,769-67,217,521 , NCBI36 chr14: 59,453,522-66,287,274 , GRCh38 chr14: 59,917,051-66,750,803	SNAPC1, ESR2, 111 more genes
nsv3924033	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 58,120,131-64,560,246 , GRCh38 chr14: 57,653,413-64,093,528 , NCBI36 chr14: 57,189,884-63,629,999	SNAPC1, DACT1, 105 more genes
nsv3902883	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863	SNAPC1, LOC440181, 1998 more genes
nsv3907460	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456	SNAPC1, BANF1P1, 1996 more genes
nsv3899639	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456	SNAPC1, LOC100289511, 1996 more genes
nsv3903256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050	SNAPC1, DHRS7, 1946 more genes
nsv3919106	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482	SNAPC1, SRMP2, 1929 more genes
nsv3904265	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229	SNAPC1, CRIP1, 1929 more genes
nsv3917422	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478	SNAPC1, MIR656, 1918 more genes
nsv6315524	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013	SNAPC1, PAPOLA-DT, 1338 more genes
nsv6637682	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 57,804,997-63,590,203 , GRCh38.p12 chr14: 57,338,279-63,123,485	SNAPC1, PARP1P2, 91 more genes
nsv5980451	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 54,654,001-75,828,024 , GRCh38.p12 chr14: 54,187,283-75,361,321	SNAPC1, ACTN1, 400 more genes
nsv4729599	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr14: 61,409,856-65,742,610 , GRCh38.p12 chr14: 60,943,138-65,275,892	SNAPC1, PARP1P2, 73 more genes
nsv3890713	copy number variation	1	nstd102	human	Benign	GRCh37 chr14: 61,898,580-62,271,175 , GRCh38.p12 chr14: 61,431,862-61,804,457	SNAPC1, LINC03033, 7 more genes
nsv4455801	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr14: 61,126,208-63,517,651 , GRCh38.p12 chr14: 60,659,490-63,050,933	SNAPC1, LOC105370529, 26 more genes
nsv4685707	copy number variation	1	nstd102	human	not provided	GRCh37 chr14: 61,701,451-62,960,957 , GRCh38.p12 chr14: 61,234,733-62,494,239	SNAPC1, LINC00644, 16 more genes
nsv4450515	copy number variation	1	nstd102	human	not provided	GRCh37 chr14: 61,701,451-62,960,957 , GRCh38.p12 chr14: 61,234,733-62,494,239	SNAPC1, LOC105370525, 16 more genes

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