vnn1[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 15

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Number of Variants: 15

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6315321	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 115,941,808-133,892,653 , GRCh37.p13 chr6: 116,262,971-134,213,791	VNN1, SLC18B1, 223 more genes
nsv3871408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 131,388,023-137,469,640 , GRCh38.p12 chr6: 131,066,883-137,148,503	VNN1, LOC105378012, 108 more genes
nsv6290946	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 130,769,034-136,009,217 , GRCh38.p12 chr6: 130,447,889-135,688,079	VNN1, LOC105378004, 89 more genes
nsv3893875	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 132,002,460-137,160,850 , GRCh38.p12 chr6: 131,681,320-136,839,712	VNN1, TAAR9, 93 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	VNN1, LOC105378061, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	VNN1, RNU6-411P, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	VNN1, SOD1P1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	VNN1, ITPR3, 2905 more genes
nsv3919111	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr6: 74,382,807-142,040,500 , NCBI36 chr6: 75,149,243-142,403,330 , GRCh37 chr6: 75,092,523-142,361,637	VNN1, RNU6-770P, 810 more genes
nsv3915150	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038	VNN1, KATNA1, 422 more genes
nsv3913689	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr6: 121,373,749-146,289,101 , GRCh37.p13 chr6: 121,332,050-146,247,408 , GRCh38.p12 chr6: 121,010,904-145,926,272	VNN1, TPD52L1, 316 more genes
nsv3896761	copy number variation	1	nstd102	human	Benign	GRCh37 chr6: 133,003,344-133,168,463 , GRCh38.p12 chr6: 132,682,205-132,847,324	VNN1, RPS12, 9 more genes
nsv3913212	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 132,776,411-133,462,292 , GRCh38 chr6: 132,455,272-133,141,153 , NCBI36 chr6: 132,818,104-133,503,985	VNN1, TAAR5, 25 more genes
nsv6290724	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 132,875,123-133,509,642 , GRCh38.p12 chr6: 132,553,984-133,188,503	VNN1, RPS12, 23 more genes
nsv4456756	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr6: 132,926,920-133,314,722 , GRCh38.p12 chr6: 132,605,781-132,993,583	VNN1, HMGB1P13, 15 more genes

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vnn1[All Fields] AND 1[has_clinical] (16)
dbVar
Fut1 [Mus caroli]
Fut1 [Mus caroli]
Gene ID:110299147

Gene

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