dbVar for Gene (Select 107986246) - 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
nsv7096733	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 520,808-1,020,391 , GRCh38.p12 chr4: 527,019-1,026,603	PDE6B-AS1, PIGG, 19 more genes
nsv6719499	copy number variation	1	nstd229	human		GRCh38 chr4: 666,959-740,658 , GRCh37.p13 chr4: 660,748-734,446	PCGF3, SLC49A3, 4 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
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
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
nsv6360524	copy number variation	1	nstd223	human		GRCh38 chr4: 715,343-814,243 , GRCh37.p13 chr4: 709,132-808,031	PCGF3-AS1, LOC105374339, 3 more genes
nsv6315440	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 114,784-47,569,569 , GRCh38.p12 chr4: 114,902-47,567,552	FAM86KP, ENPP7P11, 631 more genes
nsv6315414	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr4: 68,345-1,512,353 , GRCh38.p12 chr4: 68,453-1,510,626	ATP5ME, CTBP1, 50 more genes
nsv6315365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-5,579,467 , GRCh38.p12 chr4: 68,453-5,577,740	LOC107986246, FAM53A, 149 more genes
nsv6315347	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-20,964,575 , GRCh38.p12 chr4: 68,453-20,962,952	LOC100421802, ADRA2C, 375 more genes
nsv6315218	complex substitution	1	nstd102	human	Pathogenic	GRCh38.p12 chr4: 68,453-1,868,821 , GRCh37 chr4: 68,345-1,870,548	ATP5ME, CTBP1, 59 more genes
nsv6312255	copy number variation	2	nstd102	human	Uncertain significance	GRCh37 chr4: 493,125-3,495,228 , GRCh38.p12 chr4: 499,336-3,493,501	RN7SL671P, LOC105374343, 86 more genes
nsv6311726	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 493,125-2,065,854 , GRCh38.p12 chr4: 499,336-2,064,127	SLC49A3, LOC105374348, 51 more genes
nsv6291373	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-1,675,143 , GRCh38.p12 chr4: 68,453-1,673,416	TMED11P, DGKQ, 52 more genes

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Number of Variants: 20

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Organism

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 333

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Number of Variants: 20

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