scg5[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
nsv3872947	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr15: 32,696,494-32,712,558 , GRCh37 chr15: 32,988,695-33,004,759	SCG5, ARHGAP11A-SCG5
nsv1398183	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 32,964,938-33,004,759 , GRCh38 chr15: 32,672,737-32,712,558	SCG5, LOC105370756, 2 more genes
nsv4682234	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 32,971,947-33,004,937 , GRCh38.p12 chr15: 32,679,746-32,712,736	SCG5, LOC105370756, 1 more genes
nsv3875493	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 32,971,947-33,004,759 , GRCh38 chr15: 32,679,746-32,712,558	SCG5, LOC105370756, 1 more genes
nsv4683472	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr15: 32,971,947-32,994,756 , GRCh38.p12 chr15: 32,679,746-32,702,555	SCG5, LOC105370756, 1 more genes
nsv7094530	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,971,947-33,023,446 , GRCh38.p12 chr15: 32,679,746-32,731,245	SCG5, LOC105370756, 3 more genes
nsv7094531	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,976,738-33,023,486 , GRCh38.p12 chr15: 32,684,537-32,731,285	SCG5, LOC105370756, 3 more genes
nsv4453732	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr15: 32,684,537-32,731,255 , GRCh37 chr15: 32,976,738-33,023,456	SCG5, LOC105370756, 3 more genes
nsv7094365	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,976,738-33,023,446 , GRCh38.p12 chr15: 32,684,537-32,731,245	SCG5, GREM1-AS1, 3 more genes
nsv6309614	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,839-33,004,986 , GRCh38.p12 chr15: 32,672,638-32,712,785	SCG5, SCG5-AS1, 2 more genes
nsv5564217	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-33,004,937 , GRCh38.p12 chr15: 32,672,688-32,712,736	SCG5, SCG5-AS1, 2 more genes
nsv3883279	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,740-33,004,759 , GRCh38 chr15: 32,672,539-32,712,558	SCG5, SCG5-AS1, 2 more genes
nsv7094467	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,983,891-33,023,446 , GRCh38.p12 chr15: 32,691,690-32,731,245	SCG5, GREM1-AS1, 3 more genes
nsv5564298	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,740-33,002,449 , GRCh38.p12 chr15: 32,672,539-32,710,248	SCG5, LOC105370756, 2 more genes
nsv4682654	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,986,221-33,023,456 , GRCh38.p12 chr15: 32,694,020-32,731,255	SCG5, GREM1-AS1, 2 more genes
nsv4681499	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,988,695-33,023,446 , GRCh38.p12 chr15: 32,696,494-32,731,245	SCG5, GREM1-AS1, 2 more genes
nsv6309571	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-32,994,756 , GRCh38.p12 chr15: 32,672,688-32,702,555	SCG5, ARHGAP11A-SCG5, 2 more genes
nsv3889536	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,740-32,988,830 , GRCh38 chr15: 32,672,539-32,696,629	SCG5, LOC105370756, 2 more genes
nsv5380759	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-32,988,830 , GRCh38.p12 chr15: 32,672,688-32,696,629	SCG5, ARHGAP11A-SCG5, 2 more genes
nsv4683114	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,988,695-33,010,736 , GRCh38.p12 chr15: 32,696,494-32,718,535	SCG5, ARHGAP11A-SCG5, 2 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 101

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Number of Variants: 20

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