dbVar for Gene (Select 100506384) - 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
nsv6112778	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 51,799,648-62,916,626 , GRCh38.p12 chr20: 53,183,109-64,285,273	LINC01742, MTCO2P1, 253 more genes
nsv5022452	copy number variation	1	nstd200	human		GRCh38 chr20: 59,612,666-59,640,000 , GRCh37.p13 chr20: 58,187,721-58,215,055	, PHACTR3, 1 more genes
nsv4854068	copy number variation	1	nstd200	human		GRCh37 chr20: 58,187,721-58,215,055 , GRCh38.p12 chr20: 59,612,666-59,640,000	, PHACTR3-AS1, 1 more genes
nsv4676332	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,743,522-62,032,989 , GRCh38.p12 chr20: 57,168,466-63,401,636	BMP7, MIR298, 153 more genes
nsv4676181	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 56,788,101-62,762,405 , GRCh38.p12 chr20: 58,213,045-64,131,052	LOC105372697, MIR647, 174 more genes
nsv4357849	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,143,747-62,194,881 , GRCh38.p12 chr20: 55,568,689-63,563,528	RBM38, LAMA5, 192 more genes
nsv3920218	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 80,198-62,908,674 , GRCh38 chr20: 99,557-64,277,321 , NCBI36 chr20: 28,198-62,379,118	MIR3646, NPEPL1, 1310 more genes
nsv3916789	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 57,617,021-62,908,674 , GRCh38 chr20: 59,041,966-64,277,321 , NCBI36 chr20: 57,050,416-62,379,118	RNU7-141P, UCKL1, 153 more genes
nsv3915005	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr20: 42,849,759-62,379,118 , GRCh37 chr20: 43,416,345-62,908,674 , GRCh38 chr20: 44,787,704-64,277,321	FTLP1, RNA5SP487, 472 more genes
nsv3912982	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 53,639,062-58,949,658 , GRCh37 chr20: 54,220,678-59,516,263 , GRCh38 chr20: 55,630,597-60,941,207	ATP5F1E, BMP7, 103 more genes
nsv3911673	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 54,773,088-62,908,674 , NCBI36 chr20: 54,206,495-62,379,118 , GRCh38 chr20: 56,198,032-64,277,321	LOC105372709, NPBWR2, 226 more genes
nsv3910818	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr20: 25,616,026-62,435,964 , GRCh37.p13 chr20: 25,668,026-62,965,520 , GRCh38.p12 chr20: 25,687,390-64,334,167	RNA5SP481, LOC105372625, 855 more genes
nsv3910223	copy number variation	1	nstd102	human	Likely pathogenic	NCBI36 chr20: 51,286,111-62,385,999 , GRCh37 chr20: 51,852,704-62,915,555 , GRCh38 chr20: 53,236,165-64,284,202	ATP5F1E, BMP7, 253 more genes
nsv3910216	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 55,804,471-62,904,442 , NCBI36 chr20: 55,237,878-62,374,886 , GRCh38 chr20: 57,229,415-64,273,089	GID8, LOC105372708, 204 more genes
nsv3905072	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,948,788 , GRCh38.p12 chr20: 82,603-64,317,435	LRRN4, SNRPB, 1313 more genes
nsv3896520	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,912,463 , GRCh38.p12 chr20: 82,603-64,281,110	COMMD7, RNU7-6P, 1311 more genes
nsv3895314	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr20: 61,569-62,915,555 , GRCh38.p12 chr20: 80,928-64,284,202	PKIG, LINC01523, 1311 more genes
nsv3894116	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr20: 51,542,616-62,915,555 , GRCh38.p12 chr20: 52,926,077-64,284,202	ATP5F1E, BMP7, 254 more genes
nsv3892750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr20: 63,244-62,961,294 , GRCh38.p12 chr20: 82,603-64,329,941	TGIF2-RAB5IF, LOC105372609, 1314 more genes
nsv2112471	short tandem repeat	2	nstd128	human		GRCh37 chr20: 58,203,030-58,203,053 , GRCh38.p12 chr20: 59,627,975-59,627,998	PHACTR3, PHACTR3-AS1

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Has Clinical Interpretation

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Number of Variants: 20

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