dbVar for Gene (Select 80830) - 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
nsv5039969	copy number variation	1	nstd200	human		GRCh38 chr22: 35,640,473-35,646,418 , GRCh37.p13 chr22: 36,036,520-36,042,465	APOL6
nsv5031649	copy number variation	1	nstd200	human		GRCh38 chr22: 35,662,244-35,662,586 , GRCh37.p13 chr22: 36,058,291-36,058,633	APOL6
nsv4729926	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824	FBXO7, GTSE1, 1084 more genes
nsv4707636	copy number variation	1	nstd195	human		GRCh38.p12 chr22: 35,653,404-36,041,453 , GRCh37 chr22: 36,049,451-36,437,501 , GRCh38.p12 chr22\|NT_187630.1: 1-263,666	RPL41P3, RBFOX2, 4 more genes
nsv4676292	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 30,654,764-51,197,838 , GRCh38.p12 chr22: 30,258,775-50,759,410	PDXP-DT, PDGFB, 550 more genes
nsv4457771	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410	IGLV3-27, XKR3, 1082 more genes
nsv4292171	copy number variation	1	nstd166	human		GRCh37.p13 chr22: 36,056,195-36,056,251 , GRCh38.p12 chr22: 35,660,148-35,660,204	APOL6
nsv3922708	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 23,279,231-36,247,369 , GRCh37 chr22: 23,621,418-36,643,415 , NCBI36 chr22: 21,951,418-34,973,361	DRICH1, MMP11, 316 more genes
nsv3922128	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177	LOC102724378, CARD10, 120 more genes
nsv3919881	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079	MIR12114, MIR6820, 1059 more genes
nsv3919085	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138	IGLV2-28, LINC01310, 1023 more genes
nsv3914617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 21,261,514-37,583,387 , GRCh38 chr22: 20,907,226-37,187,347 , NCBI36 chr22: 19,591,514-35,913,333	RASL10A, SNORD125, 525 more genes
nsv3913775	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264	ZNF280A, RFPL1S, 1059 more genes
nsv3907231	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964	DDTL, PPP1R26P3, 1084 more genes
nsv3906962	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 35,728,929-51,220,961 , GRCh38.p12 chr22: 35,332,936-50,782,533	UQCRFS1P1, APOBEC3F, 435 more genes
nsv3902776	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007	LOC100419811, MTCO2P20, 1084 more genes
nsv3902598	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474	FABP5P11, SLC2A11, 1084 more genes
nsv3901960	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 23,637,907-36,614,412 , GRCh38.p12 chr22: 23,295,720-36,218,366	GRK3, NF2, 314 more genes
nsv3897008	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr22: 35,674,826-39,466,442 , GRCh38.p12 chr22: 35,278,833-39,070,437	CSF2RB, CSNK1E, 129 more genes
nsv3894026	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090	IGKV3OR22-2, ZDHHC8, 1084 more genes

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Number of Variants: 20

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Has Clinical Interpretation

Sex of Subject

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Items: 1 to 20 of 89

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Number of Variants: 20

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