slc33a1[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
nsv7096445	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 155,560,201-155,560,428 , GRCh38.p12 chr3: 155,842,412-155,842,639	SLC33A1
nsv7096941	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 155,545,999-155,560,428 , GRCh38.p12 chr3: 155,828,210-155,842,639	SLC33A1
nsv7096446	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 155,570,992-155,571,786 , GRCh38.p12 chr3: 155,853,203-155,853,997	SLC33A1, LOC105374174
nsv6313655	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 155,464,751-155,599,910 , GRCh38.p12 chr3: 155,746,962-155,882,121	SLC33A1, RPL7AP24, 3 more genes
nsv6290244	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334	SLC33A1, LOC102724145, 273 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	SLC33A1, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	SLC33A1, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	SLC33A1, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	SLC33A1, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	SLC33A1, H1-10, 846 more genes
nsv3918692	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833	SLC33A1, LOC105374179, 785 more genes
nsv3874894	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,995,020-192,997,215 , GRCh38.p12 chr3: 143,276,178-193,279,426	SLC33A1, RNU6-901P, 673 more genes
nsv3918066	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254	SLC33A1, LOC105374260, 696 more genes
nsv3918784	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013	SLC33A1, LOC105374167, 394 more genes
nsv5381765	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911	SLC33A1, MBNL1-AS1, 339 more genes
nsv4684209	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822	SLC33A1, MTAPP1, 339 more genes
nsv6290273	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295	SLC33A1, LINC02066, 206 more genes
nsv6313678	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046	SLC33A1, RNU6-901P, 229 more genes
nsv6311961	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 154,801,957-155,551,394 , GRCh38.p12 chr3: 155,084,168-155,833,605	SLC33A1, RPL7AP24, 11 more genes
nsv3911086	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 157,009,249-157,427,305 , GRCh37.p13 chr3: 155,526,555-155,944,611 , GRCh38.p12 chr3: 155,808,766-156,226,822	SLC33A1, KCNAB1, 8 more genes

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Items: 20

Number of Variants: 20

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