nek10[All Fields] AND 1[has_clinical] - dbVar - NCBI

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

Search results

Items: 18

loading data ...

Number of Variants: 18

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3887229	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 27,020,353-27,440,096 , GRCh38.p12 chr3: 26,978,862-27,398,605	NEK10, MICOS10P3, 2 more genes
nsv4674425	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 26,711,697-27,483,497 , GRCh38.p12 chr3: 26,670,206-27,442,006	NEK10, MICOS10P3, 3 more genes
nsv6636551	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 27,020,354-27,440,096 , GRCh38.p12 chr3: 26,978,863-27,398,605	NEK10, MICOS10P3, 2 more genes
nsv6311966	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779	NEK10, LOC102724104, 291 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	NEK10, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	NEK10, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	NEK10, RPL23AP49, 2875 more genes
nsv3905127	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521	NEK10, LINC02022, 540 more genes
nsv3876280	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-37,459,464 , GRCh38.p12 chr3: 20,213-37,417,973	NEK10, OXTR, 460 more genes
nsv3892895	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571	NEK10, RPL34P11, 452 more genes
nsv3878718	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-36,710,181 , GRCh38.p12 chr3: 20,213-36,668,690	NEK10, LRRC3B, 436 more genes
nsv3875913	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,891-33,958,201 , GRCh38.p12 chr3: 20,213-33,916,709	NEK10, RPS27P11, 424 more genes
nsv3901059	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703	NEK10, RPL32, 369 more genes
nsv3885169	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 16,923,595-45,249,923 , GRCh38.p12 chr3: 16,884,818-45,208,431	NEK10, RNU6-243P, 382 more genes
nsv3923656	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034	NEK10, RN7SL4P, 348 more genes
nsv3888895	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 25,045,365-32,691,140 , GRCh38.p12 chr3: 25,003,874-32,649,648	NEK10, RARB, 83 more genes
nsv4674536	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr3: 25,901,794-29,520,717 , GRCh38.p12 chr3: 25,860,303-29,479,226	NEK10, KIAA1143P2, 35 more genes
nsv3911851	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 26,926,080-28,742,419 , GRCh37.p13 chr3: 26,951,076-28,767,415 , GRCh38.p12 chr3: 26,909,585-28,725,924	NEK10, LOC105377005, 22 more genes

Supplemental Content

Filters: Manage Filters

Find related data

Search details

Recent activity

Clear Turn Off Turn On

nek10[All Fields] AND 1[has_clinical] (19)
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)