dbVar for Gene (Select 100379220) - 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
nsv7097251	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-1,843,544 , GRCh38.p12 chr4: 499,336-1,841,817	PDE6B, LOC105374339, 44 more genes
nsv7057802	inversion	1	nstd229	human		GRCh38 chr4: 1,018,368-1,160,248 , GRCh37.p13 chr4: 1,012,156-1,154,036	RNF212, LOC105374344, 4 more genes
nsv7045606	inversion	1	nstd229	human		GRCh38 chr4: 1,056,481-1,181,420 , GRCh37.p13 chr4: 1,050,269-1,175,208	RNF212, TMED11P, 3 more genes
nsv6735384	copy number variation	1	nstd229	human		GRCh38 chr4: 1,107,357-1,115,342 , GRCh37.p13 chr4: 1,101,145-1,109,130	LOC105374344, RNF212, 1 more genes
nsv6729814	copy number variation	1	nstd229	human		GRCh38 chr4: 932,438-1,207,526 , GRCh37.p13 chr4: 926,226-1,201,314	SPON2, LOC100421802, 11 more genes
nsv6720249	copy number variation	1	nstd229	human		GRCh38 chr4: 1,064,927-1,115,583 , GRCh37.p13 chr4: 1,058,715-1,109,371	LOC100421802, TMED11P, 2 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
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
nsv6629086	copy number variation	1	nstd224	human		GRCh37 chr4: 1,073,459-1,165,748 , GRCh38.p12 chr4: 1,079,671-1,171,960	RNF212, LOC105374344, 3 more genes
nsv6571930	inversion	1	nstd223	human		GRCh38 chr4: 1,056,480-1,181,419 , GRCh37.p13 chr4: 1,050,268-1,175,207	SPON2, RNF212, 3 more genes
nsv6373418	copy number variation	1	nstd223	human		GRCh38 chr4: 1,115,864-1,119,662 , GRCh37.p13 chr4: 1,109,652-1,113,450	LOC105374344, TMED11P
nsv6364193	copy number variation	1	nstd223	human		GRCh38 chr4: 715,104-1,123,703 , GRCh37.p13 chr4: 708,893-1,117,491	TMEM175, GAK, 16 more genes
nsv6362864	copy number variation	1	nstd223	human		GRCh38 chr4: 1,035,082-1,137,485 , GRCh37.p13 chr4: 1,028,870-1,131,273	LOC105374344, RNF212, 3 more genes
nsv6360166	copy number variation	1	nstd223	human		GRCh38 chr4: 999,035-1,186,087 , GRCh37.p13 chr4: 992,823-1,179,875	FGFRL1, LOC100421802, 6 more genes

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Number of Variants: 20

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Items: 1 to 20 of 318

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Number of Variants: 20

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