dbVar for Gene (Select 105372974) - 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
nsv5971197	insertion	1	nstd209	human		GRCh38 chr22: 26,244,163-26,244,163 , GRCh37.p13 chr22: 26,640,129-26,640,129	SEZ6L, SEZ6L-AS1
nsv5963119	copy number variation	1	nstd209	human		GRCh38 chr22: 26,254,007-26,254,376 , GRCh37.p13 chr22: 26,649,973-26,650,342	SEZ6L, SEZ6L-AS1
nsv5034037	copy number variation	1	nstd200	human		GRCh38 chr22: 26,234,252-26,238,952 , GRCh37.p13 chr22: 26,630,218-26,634,918	SEZ6L-AS1, SEZ6L
nsv4869265	copy number variation	1	nstd200	human		GRCh37 chr22: 26,630,218-26,634,918 , GRCh38.p12 chr22: 26,234,252-26,238,952	SEZ6L-AS1, SEZ6L
nsv4763875	insertion	1	nstd199	human		GRCh37 chr22: 26,640,133-26,640,133 , GRCh38.p12 chr22: 26,244,167-26,244,167	SEZ6L, SEZ6L-AS1
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
nsv4723087	insertion	1	nstd186	human		GRCh37 chr22: 26,640,129-26,640,129 , GRCh38.p12 chr22: 26,244,163-26,244,163	SEZ6L-AS1, SEZ6L
nsv4676280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 26,337,910-28,489,947 , GRCh38.p12 chr22: 25,941,943-28,093,959	LOC646216, MYO18B, 42 more genes
nsv4676144	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 16,888,899-27,657,507 , GRCh38.p12 chr22: 16,408,173-27,261,546	LINC02891, IGLV4-69, 466 more genes
nsv4572864	insertion	1	nstd166	human		GRCh37.p13 chr22: 26,640,129-26,640,129 , GRCh38.p12 chr22: 26,244,163-26,244,163	SEZ6L, SEZ6L-AS1
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
nsv4383389	copy number variation	1	nstd173	human		GRCh37 chr22: 21,465,662-33,984,045 , GRCh38.p12 chr22: 21,111,373-33,588,059	, XBP1, 450 more genes
nsv4316382	inversion	1	nstd166	human		GRCh37.p13 chr22: 22,466,414-30,881,792 , GRCh38.p12 chr22: 22,112,004-30,485,805	, CRYBB2, 313 more genes
nsv3924941	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr22: 26,221,273-29,477,543 , GRCh37 chr22: 26,617,239-29,873,532 , NCBI36 chr22: 24,947,239-28,203,532	TFIP11, RASL10A, 66 more genes
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
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
nsv3919429	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr22: 18,661,724-32,217,179 , GRCh38 chr22: 18,178,957-31,821,193 , NCBI36 chr22: 17,041,724-30,547,179	PCAT14, MIR3199-1, 533 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
nsv3916602	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr22: 24,411,115-26,943,393 , GRCh37 chr22: 26,081,115-28,613,393 , GRCh38 chr22: 25,685,148-28,217,405	TFIP11-DT, MIR548J, 45 more genes
nsv3915658	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr22: 23,729,059-27,359,992 , GRCh37 chr22: 25,399,059-29,029,992 , GRCh38 chr22: 25,003,092-28,634,004	GRK3, CRYBA4, 60 more genes

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Has Clinical Interpretation

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Items: 1 to 20 of 101

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Number of Variants: 20

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