slc10a4[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 18

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Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3873978	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 11,525-191,028,879 , GRCh38.p12 chr4: 11,525-190,107,724	SLC10A4, LOC100422029, 2358 more genes
nsv3876533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611	SLC10A4, LOC100420289, 2347 more genes
nsv3884499	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286	SLC10A4, MTND4LP29, 2341 more genes
nsv3880085	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318	SLC10A4, LOC112268460, 2345 more genes
nsv3883791	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495	SLC10A4, LOC105377343, 2341 more genes
nsv3872797	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-66,440,622 , GRCh38.p12 chr4: 68,453-65,574,904	SLC10A4, GNPDA2, 813 more genes
nsv7148157	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 85,624-57,073,230 , GRCh37.p13 chr4: 507,005-57,939,396	SLC10A4, OR7E84P, 764 more genes
nsv4684161	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 49,450-49,620,898 , GRCh38.p12 chr4: 49,556-49,618,881	SLC10A4, TLR10, 669 more genes
nsv7148161	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr4: 1-49,062,177 , GRCh37.p13 chr4: 507,005-49,064,194	SLC10A4, SLIRPP2, 659 more genes
nsv3876307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 12,440-49,064,044 , GRCh38.p12 chr4: 12,440-49,062,027	SLC10A4, ADGRA3, 659 more genes
nsv6634358	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	SLC10A4, LINC02475, 658 more genes
nsv3875629	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 68,345-49,089,361 , GRCh38.p12 chr4: 68,453-49,087,344	SLC10A4, LOC105374433, 658 more genes
nsv3880889	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 1,356,924-49,659,859 , GRCh38.p12 chr4: 1,363,136-49,657,842	SLC10A4, LOC107986262, 619 more genes
nsv3914335	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,358,218-63,111,600 , NCBI36 chr4: 44,052,975-62,794,195 , GRCh38 chr4: 44,356,201-62,245,882	SLC10A4, RPL22P13, 178 more genes
nsv3870878	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 38,532,827-49,064,044 , GRCh38.p12 chr4: 38,531,206-49,062,027	SLC10A4, LOC105374413, 137 more genes
nsv3923949	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 40,498,493-49,581,867 , NCBI36 chr4: 40,193,250-49,276,624 , GRCh38 chr4: 40,496,476-49,579,850	SLC10A4, CWH43, 104 more genes
nsv3922643	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr4: 44,579,695-49,083,290 , NCBI36 chr4: 44,274,452-48,778,047 , GRCh38 chr4: 44,577,678-49,081,273	SLC10A4, CWH43, 48 more genes
nsv3924494	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr4: 47,385,141-48,853,877 , GRCh38 chr4: 47,383,124-48,851,860 , NCBI36 chr4: 47,079,898-48,548,634	SLC10A4, FRYL, 24 more genes

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