sertad2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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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
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	SERTAD2, DAZAP2P1, 2991 more genes
nsv6634330	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419	SERTAD2, CYP1B1-AS1, 1649 more genes
nsv3878609	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 63,234,780-67,908,846 , GRCh38.p12 chr2: 63,007,645-67,681,714	SERTAD2, LINC02245, 80 more genes
nsv3897743	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 63,311,999-67,309,291 , GRCh37 chr2: 63,539,134-67,536,423 , NCBI36 chr2: 63,392,638-67,389,927	SERTAD2, PELI1, 68 more genes
nsv3912946	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 63,500,157-66,199,275 , GRCh37.p13 chr2: 63,646,653-66,345,771 , GRCh38.p12 chr2: 63,419,518-66,118,638	SERTAD2, CSP1, 52 more genes
nsv4453429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 63,536,353-65,793,944 , GRCh38.p12 chr2: 63,309,218-65,566,810	SERTAD2, RPS4XP5, 48 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	SERTAD2, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	SERTAD2, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	SERTAD2, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	SERTAD2, MTND2P22, 3724 more genes
nsv3916821	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 47,701,031-86,783,356 , GRCh37.p13 chr2: 47,847,527-86,929,845 , GRCh38.p12 chr2: 47,620,388-86,702,722	SERTAD2, NAGK, 595 more genes
nsv3900298	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 58,506,654-83,814,086 , GRCh38 chr2: 58,279,519-83,586,962 , NCBI36 chr2: 58,360,158-83,667,597	SERTAD2, MIR1285-2, 404 more genes
nsv3883931	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 63,671,346-85,698,002 , GRCh38.p12 chr2: 63,444,212-85,470,879	SERTAD2, LINC01888, 367 more genes
nsv6314726	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196	SERTAD2, ACTG2, 1713 more genes
nsv3903130	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr2: 64,667,733-69,956,947 , GRCh37 chr2: 64,814,229-70,103,443 , GRCh38 chr2: 64,587,095-69,876,311	SERTAD2, ANXA4, 93 more genes
nsv3885478	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr2: 61,701,437-65,731,084 , GRCh38.p12 chr2: 61,474,302-65,503,950	SERTAD2, MDH1, 80 more genes
nsv3884621	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 64,928,527-65,810,588 , GRCh38.p12 chr2: 64,701,393-65,583,454	SERTAD2, CEP68, 20 more genes
nsv3903805	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 7,635,254-88,005,418 , NCBI36 chr2: 7,552,705-87,786,533 , GRCh38 chr2: 7,495,123-87,705,899	SERTAD2, LOC101927723, 1246 more genes

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