or7d2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Number of Variants: 12

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	OR7D2, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	OR7D2, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	OR7D2, LENG8, 2408 more genes
nsv3914351	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 1,923,244-9,620,555 , GRCh38 chr19: 1,972,245-9,648,879 , GRCh37 chr19: 1,972,244-9,759,555	OR7D2, SEMA6B, 299 more genes
nsv3890584	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 3,120,160-9,732,820 , GRCh38.p12 chr19: 3,120,162-9,622,144	OR7D2, PCP2, 250 more genes
nsv3920616	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr19: 8,802,823-13,303,041 , GRCh37 chr19: 8,941,823-13,442,041 , GRCh38 chr19: 8,831,147-13,331,227	OR7D2, ACP5, 236 more genes
nsv3888397	copy number variation	1	nstd102	human	Likely pathogenic	GRCh38 chr19: 7,981,357-10,019,383 , GRCh37.p13 chr19: 8,046,241-10,130,059	OR7D2, ELAVL1, 80 more genes
nsv3907034	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 8,905,057-9,606,461 , GRCh38.p12 chr19: 8,794,381-9,495,785	OR7D2, ZNF559-ZNF177, 30 more genes
nsv4729955	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr19: 9,245,167-9,465,565 , GRCh38.p12 chr19: 9,134,491-9,354,889	OR7D2, ZNF699, 14 more genes
nsv1398241	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 8,661,944-10,104,083 , GRCh38.p12 chr19: 8,597,060-9,993,407	OR7D2, MUC16, 58 more genes
nsv4729799	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 8,518,395-10,053,298 , GRCh38.p12 chr19: 8,453,511-9,942,622	OR7D2, ZNF426-DT, 61 more genes
nsv4436244	complex substitution	1	nstd102	human	Uncertain significance	GRCh38.p12 chr19: 8,891,157-9,974,378 , GRCh37 chr19: 9,001,833-10,085,054	OR7D2, PIN1, 51 more genes

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