dbVar for OMIM (Select 191170) - 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
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	LOC105370756, 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-AS1, ARHGAP11A-SCG5, 2 more genes
nsv5380920	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-33,012,502 , GRCh38.p12 chr15: 32,672,688-32,720,301	GREM1-AS1, LOC105370756, 4 more genes
nsv5380836	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-33,010,412 , GRCh38.p12 chr15: 32,672,688-32,718,211	GREM1-AS1, ARHGAP11A-SCG5, 4 more genes
nsv5380760	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-33,010,736 , GRCh38.p12 chr15: 32,672,688-32,718,535	GREM1-AS1, LOC105370756, 4 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
nsv5380758	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289	LOC105370794, HNRNPA1P45, 1173 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
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	ARHGAP11A-SCG5, GREM1, 2 more genes
nsv4683112	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,889-33,023,446 , GRCh38.p12 chr15: 32,672,688-32,731,245	GREM1, SCG5-AS1, 4 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	GREM1-AS1, ARHGAP11A-SCG5, 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
nsv4681637	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr15: 32,964,740-32,972,136 , GRCh38.p12 chr15: 32,672,539-32,679,935	ARHGAP11A-SCG5, SCG5, 1 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	GREM1-AS1, SCG5, 2 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	LOC105370756, SCG5, 3 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	LOC105370756, SCG5, 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-AS1, SCG5, 2 more genes
nsv3877866	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr15: 32,672,539-32,731,255 , GRCh37 chr15: 32,964,740-33,023,456	GREM1-AS1, SCG5, 4 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
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

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Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

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Items: 1 to 20 of 21

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Number of Variants: 20

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