efcab5[All Fields] AND 1[has_clinical] - dbVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 17

loading data ...

Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3900887	copy number variation	1	nstd102	human	Benign	GRCh37 chr17: 28,285,845-28,336,772 , GRCh38.p12 chr17: 29,958,827-30,009,754	EFCAB5
nsv4730022	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 28,263,607-28,338,007 , GRCh38.p12 chr17: 29,936,589-30,010,989	EFCAB5
nsv4457560	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 28,287,734-28,338,006 , GRCh38.p12 chr17: 29,960,716-30,010,988	EFCAB5
nsv3919950	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 24,298,969-27,841,151 , GRCh37 chr17: 27,274,843-30,817,038 , GRCh38 chr17: 28,947,825-32,490,020	EFCAB5, MIR365B, 105 more genes
nsv7095086	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 27,573,882-29,576,157 , GRCh38.p12 chr17: 29,246,864-31,249,139	EFCAB5, LOC107984990, 59 more genes
nsv3903684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004	EFCAB5, MIR3185, 2366 more genes
nsv3899740	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564	EFCAB5, P4HB, 2366 more genes
nsv3906245	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251	EFCAB5, MIR21, 2366 more genes
nsv3907261	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062	EFCAB5, SMURF2, 2366 more genes
nsv3914783	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577	EFCAB5, LOC105371922, 1855 more genes
nsv4457831	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395	EFCAB5, LOC105371753, 474 more genes
nsv6314042	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 21,690,653-28,281,232 , GRCh38.p12 chr17: 22,164,047-29,954,214	EFCAB5, TAOK1, 131 more genes
nsv4675321	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 25,274,363-28,450,707 , GRCh38.p12 chr17: 26,947,337-30,123,689	EFCAB5, ABHD15, 112 more genes
nsv3972367	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 25,403,446-31,685,464 , GRCh38.p12 chr17: 27,076,420-33,358,446	EFCAB5, ASIC2, 190 more genes
nsv3903658	copy number variation	1	nstd102	human	drug response	GRCh37 chr17: 25,248,166-30,645,676 , GRCh38.p12 chr17: 26,935,981-32,318,657	EFCAB5, KRT18P55, 179 more genes
nsv7095084	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 26,684,694-29,701,173 , GRCh38.p12 chr17: 28,357,671-31,374,155	EFCAB5, RNU6-1267P, 114 more genes
nsv3916884	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr17: 24,137,711-25,589,217 , GRCh37.p13 chr17: 27,113,585-28,565,091 , GRCh38.p12 chr17: 28,786,567-30,238,073	EFCAB5, MIR451B, 43 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

efcab5[All Fields] AND 1[has_clinical] (18)
dbVar

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)