amz2[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
nsv3911811	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577	AMZ2, PRPSAP1, 1350 more genes
nsv3921398	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 65,829,982-68,081,995 , GRCh38 chr17: 67,833,866-70,085,854 , NCBI36 chr17: 63,260,444-65,593,590	AMZ2, LRRC37A16P, 41 more genes
nsv3920127	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 67,584,224-68,639,875 , NCBI36 chr17: 63,010,802-64,147,611 , GRCh37 chr17: 65,580,340-66,636,016	AMZ2, LOC101928045, 25 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	AMZ2, 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	AMZ2, 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	AMZ2, 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	AMZ2, 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	AMZ2, LOC105371922, 1855 more genes
nsv3909511	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846	AMZ2, FOXK2, 958 more genes
nsv3913552	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225	AMZ2, RNU6-131P, 1075 more genes
nsv4457646	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062	AMZ2, LOC107985089, 448 more genes
nsv3909523	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062	AMZ2, RPL38, 428 more genes
nsv4457799	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302	AMZ2, PECAM1, 215 more genes
nsv4349383	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr17: 57,357,088-66,306,668 , GRCh38.p12 chr17: 59,279,727-68,310,527	AMZ2, FAM136DP, 214 more genes
nsv3972399	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr17: 64,159,738-74,891,024 , GRCh38.p12 chr17: 66,163,620-76,894,942	AMZ2, AANAT, 243 more genes
nsv6637738	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 66,075,889-66,268,460 , GRCh38.p12 chr17: 68,079,784-68,272,319	AMZ2, ARSG, 8 more genes
nsv3902629	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr17: 65,343,022-69,344,022 , GRCh38.p12 chr17: 67,346,906-71,347,881	AMZ2, RN7SL622P, 59 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

amz2[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)