dbVar for Gene (Select 100616226) - 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
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
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
nsv4728895	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 137,658,677-137,982,831 , GRCh38.p12 chr7: 137,973,931-138,298,086	LOC107986749, CREB3L2, 7 more genes
nsv4676044	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 135,677,938-139,810,886 , GRCh38.p12 chr7: 135,993,190-140,111,086	SVOPL, RPS17P12, 62 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
nsv4675615	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620	ATG9B, OR10AC1, 603 more genes
nsv4457201	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 137,675,423-139,084,024 , GRCh38.p12 chr7: 137,990,677-139,399,278	ZC3HAV1L, TRR-CCT4-1, 34 more genes
nsv4457085	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 134,648,448-137,942,208 , GRCh38.p12 chr7: 134,963,697-138,257,463	PSMC1P3, TMEM140, 45 more genes
nsv4455493	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 130,592,554-159,119,707 , GRCh38.p12 chr7: 130,907,795-159,327,017	OR2A1, LOC101027084, 614 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
nsv4436127	complex substitution	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 129,367,205-140,482,957 , GRCh38.p12 chr7: 129,727,365-140,783,157	AKR1B1, BPGM, 187 more genes
nsv4349183	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530	LOC105375582, TRBJ2-4, 686 more genes
nsv4167481	copy number variation	1	nstd166	human		GRCh37.p13 chr7: 137,605,467-137,997,146 , GRCh38.p12 chr7: 137,920,721-138,312,401	LOC107986749, CREB3L2, 8 more genes
nsv3924585	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 130,506,777-158,812,468 , GRCh38 chr7: 131,171,478-159,327,017 , GRCh37 chr7: 130,856,237-159,119,707	PAXBP1P1, RNY3, 611 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
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
nsv3919545	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 130,564,063-158,821,317 , GRCh37 chr7: 130,913,523-159,128,556 , GRCh38 chr7: 131,228,764-159,335,866	LOC105375594, CLCN1, 611 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

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Number of Variants: 20

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