dbVar for Gene (Select 168433) - 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
nsv5556846	sequence alteration	1	nstd206	human		GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670	, AHR, 2675 more genes
nsv5381759	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640	TMEM229A, ST7-OT3, 110 more genes
nsv5326600	inversion	1	nstd204	human		GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904	, ARF5, 752 more genes
nsv5039775	inversion	1	nstd200	human		GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114	, NFE4, 1832 more genes
nsv5029742	inversion	1	nstd200	human		GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680	, LOC100533722, 1168 more genes
nsv4880762	inversion	1	nstd200	human		GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588	, RN7SKP277, 1168 more genes
nsv4675620	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017	RPL26P23, ST13P17, 887 more genes
nsv4675322	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860	CBLL1-AS1, COMETT, 168 more genes
nsv4455826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163	ASB15, PNPT1P2, 127 more genes
nsv4455091	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017	RPL23AP51, FLJ40288, 2684 more genes
nsv3923694	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 122,291,571-122,684,719 , GRCh38 chr7: 122,651,517-123,044,665 , NCBI36 chr7: 122,078,807-122,471,955	TAS2R16, CADPS2, 5 more genes
nsv3923570	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 107,583,881-122,963,817 , GRCh37.p13 chr7: 107,796,645-123,176,581 , GRCh38.p12 chr7: 108,156,200-123,536,527	ANKRD7, NDUFA5, 142 more genes
nsv3923381	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 121,101,368-122,522,849 , NCBI36 chr7: 120,888,604-122,310,085 , GRCh38 chr7: 121,461,314-122,882,795	LOC105375481, LOC102724527, 15 more genes
nsv3923164	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 121,658,176-128,547,780 , GRCh38 chr7: 122,018,122-128,907,727 , NCBI36 chr7: 121,445,412-128,335,016	GCC1, RNF133, 104 more genes
nsv3922815	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 96,887,100-158,409,214 , GRCh38 chr7: 97,419,852-158,923,762 , GRCh37 chr7: 97,049,164-158,716,453	SEPTIN7P6, MIR93, 1175 more genes
nsv3922792	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 113,227,126-124,326,508 , GRCh37 chr7: 113,439,890-124,539,272 , GRCh38 chr7: 113,799,835-124,899,218	MTND4P6, COMETT, 116 more genes
nsv3919826	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 54,185-159,075,079 , GRCh38 chr7: 54,185-159,282,390 , NCBI36 chr7: 149,268-158,767,840	RNU6-438P, LOC105375300, 2682 more genes
nsv3918979	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 115,099,069-159,118,507 , NCBI36 chr7: 114,886,305-158,811,268 , GRCh38 chr7: 115,459,015-159,325,817	ABCF2, LOC105375581, 844 more genes
nsv3917337	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 121,863,759-159,335,865 , NCBI36 chr7: 121,291,049-158,821,316 , GRCh37 chr7: 121,503,813-159,128,555	INSIG1-DT, RBM33, 776 more genes
nsv3917215	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr7: 122,113,100-122,158,830 , GRCh37 chr7: 122,325,864-122,371,594 , GRCh38 chr7: 122,685,810-122,731,540	RNF148, CADPS2, 1 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 102

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Number of Variants: 20

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