sema3c[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
nsv4456795	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 80,427,529-80,557,198 , GRCh38.p12 chr7: 80,798,213-80,927,882	SEMA3C
nsv4675525	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 80,303,798-80,744,443 , GRCh38.p12 chr7: 80,674,482-81,115,127	SEMA3C, CD36
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	SEMA3C, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	SEMA3C, LOC107986817, 2014 more genes
nsv3918722	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 71,225,344-81,735,657 , GRCh37 chr7: 70,690,330-81,364,973 , NCBI36 chr7: 70,328,266-81,202,909	SEMA3C, GTF2IP1, 184 more genes
nsv3922762	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 73,992,744-83,618,176 , GRCh38 chr7: 73,873,420-83,988,860 , NCBI36 chr7: 72,925,686-83,456,112	SEMA3C, PMS2P3, 142 more genes
nsv3917211	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 74,377,395-82,031,742 , NCBI36 chr7: 73,429,661-81,498,994 , GRCh37 chr7: 73,992,744-81,661,058	SEMA3C, HSPB1, 123 more genes
nsv6313880	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 77,310,644-84,461,089 , GRCh38.p12 chr7: 77,681,327-84,831,773	SEMA3C, RNU6-337P, 54 more genes
nsv6312357	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 80,276,057-83,739,925 , GRCh38.p12 chr7: 80,646,741-84,110,609	SEMA3C, LOC107986813, 19 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	SEMA3C, RNU6-565P, 2684 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	SEMA3C, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	SEMA3C, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	SEMA3C, TRGV3, 2682 more genes
nsv6313801	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 77,821,356-93,340,137 , GRCh38.p12 chr7: 78,192,039-93,710,825	SEMA3C, SOCS5P1, 140 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	SEMA3C, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	SEMA3C, ACHE, 1532 more genes
nsv3878310	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 79,337,679-86,790,392 , GRCh38 chr7: 79,708,363-87,161,076	SEMA3C, CACNA2D1, 48 more genes
nsv3898444	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 80,348,675-83,666,606 , GRCh38.p12 chr7: 80,719,359-84,037,290	SEMA3C, CACNA2D1, 18 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	SEMA3C, RRBP1P1, 2680 more genes
nsv3873500	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 73,591,993-93,683,437 , GRCh38.p12 chr7: 74,177,663-94,054,125	SEMA3C, LOC645324, 242 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 24

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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