sec16b[All Fields] AND 1[has_clinical] - 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
nsv3912840	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,764,751-247,199,719 , GRCh37.p13 chr1: 146,053,394-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	SEC16B, CRB1, 1608 more genes
nsv3874431	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 171,990,029-195,086,758 , GRCh38.p12 chr1: 172,020,889-195,117,628	SEC16B, PTGS2, 307 more genes
nsv3873192	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 161,676,893-184,071,723 , GRCh38.p12 chr1: 161,707,103-184,102,589	SEC16B, COLGALT2, 402 more genes
nsv4673925	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 177,551,193-199,599,056 , GRCh38.p12 chr1: 177,582,058-199,629,928	SEC16B, QSOX1, 263 more genes
nsv3904393	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 170,898,861-191,034,539 , GRCh38 chr1: 170,929,720-191,065,409 , NCBI36 chr1: 169,165,485-189,301,162	SEC16B, RPL18P2, 302 more genes
nsv3896481	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 176,595,962-196,301,688 , GRCh37 chr1: 176,565,098-196,270,818 , NCBI36 chr1: 174,831,721-194,537,441	SEC16B, RN7SL230P, 231 more genes
nsv3901149	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 168,271,833-185,790,903 , GRCh37 chr1: 170,005,209-187,524,280 , GRCh38 chr1: 170,036,068-187,555,148	SEC16B, RGSL1, 296 more genes
nsv3886667	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 173,131,908-187,406,532 , GRCh38.p12 chr1: 173,162,769-187,437,400	SEC16B, CRYZL2P, 233 more genes
nsv3885424	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 169,873,155-181,823,980 , GRCh38.p12 chr1: 169,904,014-181,854,845	SEC16B, TRUND-NNN7-1, 210 more genes
nsv3907850	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 175,035,040-186,042,595 , NCBI36 chr1: 173,270,799-184,278,350 , GRCh37 chr1: 175,004,176-186,011,727	SEC16B, LOC100129573, 172 more genes
nsv4436225	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 172,652,343-183,538,289 , GRCh38.p12 chr1: 172,683,203-183,569,154	SEC16B, KIAA1614-AS1, 190 more genes
nsv3887418	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 172,742,952-181,814,496 , GRCh38.p12 chr1: 172,773,812-181,845,361	SEC16B, ZBTB37, 152 more genes
nsv3896314	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 169,187,474-178,044,969 , NCBI36 chr1: 167,454,098-176,311,592 , GRCh38 chr1: 169,218,236-178,075,834	SEC16B, RPS26P12, 150 more genes
nsv3877365	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 47,851-249,228,449 , GRCh38.p12 chr1: 47,851-248,934,250	SEC16B, MARK1, 4930 more genes
nsv3885206	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-249,218,992 , GRCh38.p12 chr1: 82,154-248,924,793	SEC16B, SNAP47, 4927 more genes
nsv3884414	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-249,224,684 , GRCh38.p12 chr1: 914,087-248,930,485	SEC16B, RNU1-153P, 4887 more genes
nsv3918947	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 144,475,856-247,199,719 , GRCh37.p13 chr1: 145,764,499-249,233,096 , GRCh38.p12 chr1: 120,836,007-206,268,643	SEC16B, LOC101060227, 1608 more genes
nsv3900459	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 149,854,269-180,267,197 , NCBI36 chr1: 148,092,455-178,502,955 , GRCh37 chr1: 149,825,831-180,236,332	SEC16B, HORMAD1, 923 more genes
nsv3898042	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 171,009,116-186,845,089 , NCBI36 chr1: 169,275,740-185,111,712 , GRCh38 chr1: 171,039,975-186,875,957	SEC16B, XPR1, 279 more genes
nsv3896331	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 164,922,655-180,061,589 , NCBI36 chr1: 163,158,516-178,297,347 , GRCh37 chr1: 164,891,892-180,030,724	SEC16B, GAS5-AS1, 290 more genes

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Number of Variants: 20

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 25

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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