c7orf57[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3911000	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 48,018,144-48,135,497 , GRCh38 chr7: 48,012,022-48,129,375 , GRCh37 chr7: 48,051,619-48,168,972	C7ORF57, LOC105375271, 2 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	C7ORF57, RNU6-438P, 2682 more genes
nsv3888815	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 12,258,147-140,494,267 , GRCh38.p12 chr7: 12,218,521-140,794,467	C7ORF57, LOC107986817, 2014 more genes
nsv3924054	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,573,756-56,174,815 , NCBI36 chr7: 40,540,281-56,142,309 , GRCh38 chr7: 40,534,157-56,107,122	C7ORF57, VOPP1-DT, 229 more genes
nsv3916442	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 37,309,607-48,670,880 , GRCh37 chr7: 37,343,082-48,700,334 , GRCh38 chr7: 37,303,478-48,660,738	C7ORF57, LOC102724903, 204 more genes
nsv3911166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,060,197-50,611,198 , NCBI36 chr7: 40,026,722-50,578,692 , GRCh38 chr7: 40,020,598-50,543,500	C7ORF57, SUGCT, 155 more genes
nsv6313509	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060	C7ORF57, LINC01447, 142 more genes
nsv3919937	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 44,571,949-53,699,760 , GRCh37 chr7: 44,611,548-53,767,453 , NCBI36 chr7: 44,578,073-53,734,947	C7ORF57, LOC105375262, 106 more genes
nsv5381787	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,341,583-50,171,623 , GRCh38.p12 chr7: 43,301,984-50,132,027	C7ORF57, OGDH, 110 more genes
nsv3894780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 10,704-159,122,532 , GRCh38.p12 chr7: 10,704-159,329,842	C7ORF57, RNU6-565P, 2684 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	C7ORF57, RPL23AP51, 2684 more genes
nsv3909087	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 44,935-159,126,310 , GRCh38.p12 chr7: 44,935-159,333,620	C7ORF57, MNX1-AS2, 2682 more genes
nsv3908592	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr7: 43,361-159,119,707 , GRCh38.p12 chr7: 43,361-159,327,017	C7ORF57, TRGV3, 2682 more genes
nsv3899194	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 11,048,840-52,863,626 , GRCh38.p12 chr7: 11,009,213-52,795,933	C7ORF57, BRWD1P3, 590 more genes
nsv3917263	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 33,328,312-62,377,476 , GRCh37 chr7: 33,367,924-61,831,899 , NCBI36 chr7: 33,334,449-61,469,334	C7ORF57, MIR4649, 444 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	C7ORF57, AOC1, 2682 more genes
nsv4352523	inversion	1	nstd102	human	Pathogenic	GRCh37 chr7: 20,954,043-114,556,605 , GRCh38.p12 chr7: 20,914,424-114,916,550	C7ORF57, ACHE, 1532 more genes
nsv6634332	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635	C7ORF57, RRBP1P1, 2680 more genes
nsv3923104	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr7: 47,849,282-48,162,394 , GRCh38 chr7: 47,843,159-48,156,272 , GRCh37 chr7: 47,882,757-48,195,869	C7ORF57, PKD1L1, 5 more genes

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