tlx3[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
nsv3889848	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719	TLX3, MEGF10, 2080 more genes
nsv3879307	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 164,207,156-172,799,124 , GRCh38.p12 chr5: 164,780,150-173,372,121	TLX3, RN7SL339P, 113 more genes
nsv4578263	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841	TLX3, LINC01187, 112 more genes
nsv3886374	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028	TLX3, LOC105374618, 2499 more genes
nsv3871533	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343	TLX3, PCDHGC5, 2492 more genes
nsv3875235	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788	TLX3, SPEF2, 2490 more genes
nsv3874238	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 106,716,357-180,687,338 , GRCh38.p12 chr5: 107,380,656-181,260,337	TLX3, PJA2, 1228 more genes
nsv6315448	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788	TLX3, GRM6, 554 more genes
nsv3921182	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 149,094,155-180,699,152 , GRCh38 chr5: 149,714,592-181,272,151 , NCBI36 chr5: 149,074,348-180,631,758	TLX3, RN7SKP148, 553 more genes
nsv3885523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 155,344,802-180,693,344 , GRCh38.p12 chr5: 155,917,792-181,266,343	TLX3, WWC1, 446 more genes
nsv3924400	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 156,185,101-180,629,412 , GRCh37 chr5: 156,252,523-180,696,806 , GRCh38 chr5: 156,825,512-181,269,805	TLX3, CEP192P1, 443 more genes
nsv6636891	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790	TLX3, EFCAB9, 287 more genes
nsv3921186	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr5: 164,386,701-181,269,805 , GRCh37 chr5: 163,813,707-180,696,806 , NCBI36 chr5: 163,746,285-180,629,412	TLX3, TENM2, 347 more genes
nsv3920339	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr5: 164,323,950-180,629,412 , GRCh37.p13 chr5: 164,391,372-180,696,806 , GRCh38.p12 chr5: 164,964,366-181,269,805	TLX3, MIR1229, 343 more genes
nsv4455586	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 156,597,181-171,166,353 , GRCh38.p12 chr5: 157,170,170-171,739,349	TLX3, LOC105377677, 164 more genes
nsv3918887	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 168,761,759-180,712,302 , NCBI36 chr5: 168,694,337-180,644,908 , GRCh38 chr5: 169,334,755-181,285,301	TLX3, RPS8P7, 311 more genes
nsv6634369	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788	TLX3, GFPT2, 287 more genes
nsv3884275	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr5: 94,844,077-178,830,410 , GRCh38.p12 chr5: 95,508,373-179,403,409	TLX3, LOC107986368, 1258 more genes
nsv3914475	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr5: 167,860,417-170,844,183 , GRCh38 chr5: 168,433,412-171,417,179 , NCBI36 chr5: 167,792,995-170,776,788	TLX3, INSYN2B, 48 more genes
nsv3912593	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259	TLX3, LOC105378993, 2492 more genes

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Items: 20

Number of Variants: 20

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