slc12a9[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
nsv7097098	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,410,349-100,424,652 , GRCh38.p12 chr7: 100,812,727-100,827,030	SLC12A9, RN7SL750P, 1 more genes
nsv6312416	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr7: 100,411,521-100,424,652 , GRCh38.p12 chr7: 100,813,899-100,827,030	SLC12A9, EPHB4, 1 more genes
nsv3903677	copy number variation	1	nstd102	human	Benign	GRCh37 chr7: 100,367,573-100,457,578 , GRCh38.p12 chr7: 100,769,950-100,859,956	SLC12A9, SLC12A9-AS1, 3 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, MUC17, 135 more genes
nsv3919108	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr7: 100,419,914-102,482,826 , NCBI36 chr7: 99,855,473-101,910,278 , GRCh37 chr7: 100,017,537-102,123,273	SLC12A9, SPACDR, 80 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, CYP3A5, 1144 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	SLC12A9, 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	SLC12A9, 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	SLC12A9, ACHE, 1532 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 26

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Number of Variants: 20

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