dbVar for Gene (Select 100506858) - 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
nsv6112732	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,200-4,012,072 , GRCh38.p12 chr5: 13,200-4,011,958	SLC9A3-AS1, LOC107984098, 76 more genes
nsv5904189	copy number variation	1	nstd209	human		GRCh38 chr5: 2,305,973-2,307,101 , GRCh37.p13 chr5: 2,306,087-2,307,215	LOC100506858
nsv5842580	copy number variation	1	nstd209	human		GRCh38 chr5: 2,305,756-2,307,187 , GRCh37.p13 chr5: 2,305,870-2,307,301	LOC100506858
nsv5471629	copy number variation	1	nstd206	human		GRCh38 chr5: 2,290,000-2,339,000 , GRCh37.p13 chr5: 2,290,114-2,339,114	LOC100506858
nsv5470931	copy number variation	1	nstd206	human		GRCh38 chr5: 2,305,974-2,307,102 , GRCh37.p13 chr5: 2,306,088-2,307,216	LOC100506858
nsv5465832	copy number variation	1	nstd206	human		GRCh38 chr5: 2,302,962-2,308,257 , GRCh37.p13 chr5: 2,303,076-2,308,371	LOC100506858
nsv5381771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 22,149-29,048,823 , GRCh38.p12 chr5: 22,149-29,048,716	OTULINL, AKTIPP2, 317 more genes
nsv4808521	copy number variation	1	nstd200	human		GRCh37 chr5: 2,306,088-2,307,216 , GRCh38.p12 chr5: 2,305,974-2,307,102	LOC100506858
nsv4728897	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-4,305,172 , GRCh38.p12 chr5: 113,461-4,305,059	PPP4R2P1, MIR6075, 75 more genes
nsv4685752	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 71,904-22,078,969 , GRCh38.p12 chr5: 71,789-22,078,860	LINC01377, LOC100421308, 277 more genes
nsv4674705	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-5,657,333 , GRCh38.p12 chr5: 113,461-5,657,220	LOC101929898, MIR4635, 90 more genes
nsv4674549	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-4,325,585 , GRCh38.p12 chr5: 113,461-4,325,472	LINC01017, LOC105374614, 75 more genes
nsv4674497	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-14,738,180 , GRCh38.p12 chr5: 113,461-14,738,071	LOC101929003, MTCYBP37, 192 more genes
nsv4674444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 1,322,680-10,762,544 , GRCh38.p12 chr5: 1,322,565-10,762,432	LOC100132773, LINC01019, 125 more genes
nsv4674387	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 113,576-2,485,820 , GRCh38.p12 chr5: 113,461-2,485,706	LOC105374614, LOC112267946, 58 more genes
nsv4674161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-23,364,376 , GRCh38.p12 chr5: 113,461-23,364,267	LOC102723561, LOC107986397, 287 more genes
nsv4674139	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-5,194,484 , GRCh38.p12 chr5: 113,461-5,194,371	BRD9, LOC100310782, 84 more genes
nsv4674130	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 113,576-11,767,720 , GRCh38.p12 chr5: 113,461-11,767,608	SLC9A3-AS1, LINC02114, 169 more genes
nsv4396134	copy number variation	1	nstd174	human		GRCh37 chr5: 2,306,070-2,307,255 , GRCh38.p12 chr5: 2,305,956-2,307,141	LOC100506858
nsv4369315	copy number variation	1	nstd173	human		GRCh37 chr5: 113,577-10,304,966 , GRCh38.p12 chr5: 113,462-10,304,854	, LOC105374625, 158 more genes

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Items: 1 to 20 of 260

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Number of Variants: 20

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