dbVar for Gene (Select 79441) - 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
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLIRPP2, STIM2-AS1, 659 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	OR7E84P, FAM193A, 764 more genes
nsv7137196	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-34,512,694 , GRCh38.p12 chr4: 68,453-34,511,072	ECM1P2, LOC105378240, 482 more genes
nsv7049289	inversion	1	nstd229	human		GRCh38 chr4: 1,879,237-2,966,412 , GRCh37.p13 chr4: 1,880,964-2,968,139	RNF4, SCARNA22, 28 more genes
nsv7039441	inversion	1	nstd229	human		GRCh38 chr4: 1,689,472-2,959,448 , GRCh37.p13 chr4: 1,691,199-2,961,175	NOP14-AS1, LOC112268460, 34 more genes
nsv6730394	copy number variation	1	nstd229	human		GRCh38 chr4: 2,200,486-2,609,402 , GRCh37.p13 chr4: 2,202,213-2,611,129	MIR4800, LOC105374352, 13 more genes
nsv6726871	copy number variation	1	nstd229	human		GRCh38 chr4: 2,234,148-2,235,473 , GRCh37.p13 chr4: 2,235,875-2,237,200	COX6B1P5, HAUS3, 1 more genes
nsv6725535	copy number variation	1	nstd229	human		GRCh38 chr4: 2,201,001-2,480,600 , GRCh37.p13 chr4: 2,202,728-2,482,327	POLN, RNF4, 12 more genes
nsv6721069	copy number variation	1	nstd229	human		GRCh38 chr4: 2,239,914-2,242,535 , GRCh37.p13 chr4: 2,241,641-2,244,262	POLN, COX6B1P5, 1 more genes
nsv6720602	copy number variation	1	nstd229	human		GRCh38 chr4: 2,242,604-2,242,642 , GRCh37.p13 chr4: 2,244,331-2,244,369	HAUS3, POLN
nsv6637013	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 2,195,665-2,503,033 , GRCh38.p12 chr4: 2,193,938-2,501,306	LOC105374352, POLN, 12 more genes
nsv6636691	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-2,437,290 , GRCh38.p12 chr4: 68,454-2,435,563	SPON2, TACC3, 77 more genes
nsv6636600	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 1,892,740-2,503,033 , GRCh38.p12 chr4: 1,891,013-2,501,306	LOC105374352, POLN, 19 more genes
nsv6636582	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-12,369,983 , GRCh38.p12 chr4: 68,454-12,368,359	NELFA, OR7E111FP, 289 more genes
nsv6636534	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 963,688-2,913,553 , GRCh38.p12 chr4: 969,900-2,911,826	ADD1, CTBP1, 53 more genes
nsv6636256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1-12,785,001 , GRCh38.p12 chr4: 10,001-12,783,377	AFAP1-AS1, LOC389199, 294 more genes
nsv6634358	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	LINC02475, LOC105374344, 658 more genes
nsv6629848	copy number variation	5	nstd224	human		GRCh37 chr4: 2,233,709-2,252,881 , GRCh38.p12 chr4: 2,231,982-2,251,154	POLN, COX6B1P5, 3 more genes
nsv6629847	copy number variation	1	nstd224	human		GRCh37 chr4: 2,230,842-2,242,588 , GRCh38.p12 chr4: 2,229,115-2,240,861	HAUS3, POLN, 1 more genes
nsv6629475	copy number variation	2	nstd224	human		GRCh37 chr4: 2,209,749-2,242,588 , GRCh38.p12 chr4: 2,208,022-2,240,861	POLN, HAUS3, 1 more genes

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Items: 1 to 20 of 327

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Number of Variants: 20

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