ap4m1[All Fields] AND 1[has_clinical] - 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
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	AP4M1, 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	AP4M1, LOC107986817, 2014 more genes
nsv6313503	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 99,417,471-111,586,308 , GRCh38.p12 chr7: 99,819,848-111,946,253	AP4M1, GJC3, 237 more genes
nsv3903311	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,847,725-102,472,176 , GRCh38.p12 chr7: 99,250,102-102,831,729	AP4M1, PLOD3, 163 more genes
nsv3915692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 99,195,836-102,258,175 , NCBI36 chr7: 98,631,395-101,688,175 , GRCh37 chr7: 98,793,459-101,718,950	AP4M1, MUC17, 135 more genes
nsv7148181	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421	AP4M1, LAMTOR4, 107 more genes
nsv6312372	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,983,338-100,860,555 , GRCh38.p12 chr7: 99,385,715-101,217,274	AP4M1, AZGP1P1, 119 more genes
nsv3915383	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr7: 98,654,979-100,337,825 , GRCh38 chr7: 99,219,420-100,902,269 , GRCh37 chr7: 98,817,043-100,499,889	AP4M1, GNB2, 104 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	AP4M1, 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	AP4M1, 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	AP4M1, 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	AP4M1, TRGV3, 2682 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	AP4M1, SEPTIN7P6, 1175 more genes
nsv3894097	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 98,693,388-159,119,707 , GRCh38.p12 chr7: 99,095,765-159,327,017	AP4M1, CYP3A5, 1144 more genes
nsv5381780	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704	AP4M1, ARPC1A, 265 more genes
nsv3916333	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 97,917,786-100,903,085 , GRCh38 chr7: 98,288,474-101,259,804 , NCBI36 chr7: 97,755,722-100,689,805	AP4M1, ZCWPW1, 141 more genes
nsv6315223	complex substitution	1	nstd102	human	Pathogenic	GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017	AP4M1, 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	AP4M1, ACHE, 1532 more genes
nsv4684274	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr7: 99,593,346-102,470,275 , GRCh38.p12 chr7: 99,995,723-102,829,828	AP4M1, ACHE, 124 more genes
nsv3922535	copy number variation	1	nstd102	human	Likely benign	NCBI36 chr7: 98,631,395-99,783,622 , GRCh37 chr7: 98,793,459-99,945,686 , GRCh38 chr7: 99,195,836-100,348,063	AP4M1, LAMTOR4, 66 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 25

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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