KIAA1614[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
nsv4453631	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr1: 180,606,386-180,915,350 , GRCh38.p12 chr1: 180,637,250-180,946,214	KIAA1614, XPR1, 2 more genes
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	KIAA1614, 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	KIAA1614, 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	KIAA1614, COLGALT2, 402 more genes
nsv3888143	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,413,479-201,764,737 , GRCh38.p12 chr1: 179,444,344-201,795,609	KIAA1614, CSRP1-AS1, 273 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	KIAA1614, QSOX1, 263 more genes
nsv3878624	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,073,386-200,192,265 , GRCh38.p12 chr1: 179,104,251-200,223,137	KIAA1614, LOC105371661, 249 more genes
nsv3905741	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,002,040-199,694,025 , NCBI36 chr1: 177,268,663-197,960,648 , GRCh38 chr1: 179,032,905-199,724,897	KIAA1614, SLC4A1APP2, 240 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	KIAA1614, RPL18P2, 302 more genes
nsv3877653	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,011,314-199,022,759 , GRCh38.p12 chr1: 179,042,179-199,053,630	KIAA1614, LINC02818, 234 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	KIAA1614, 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	KIAA1614, 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	KIAA1614, CRYZL2P, 233 more genes
nsv6637124	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,727,182-192,260,142 , GRCh38.p12 chr1: 179,758,047-192,291,012	KIAA1614, LOC101928933, 148 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	KIAA1614, TRUND-NNN7-1, 210 more genes
nsv6290451	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 178,522,021-190,322,133 , GRCh38.p12 chr1: 178,552,886-190,353,003	KIAA1614, RNU7-13P, 167 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	KIAA1614, 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	KIAA1614, 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	KIAA1614, ZBTB37, 152 more genes
nsv3885166	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 179,564,752-183,850,820 , GRCh38.p12 chr1: 179,595,617-183,881,686	KIAA1614, RPL18P2, 78 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 36

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Number of Variants: 20

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