ankrd45[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	ANKRD45, 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	ANKRD45, 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	ANKRD45, COLGALT2, 402 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	ANKRD45, RPL18P2, 302 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	ANKRD45, RGSL1, 296 more genes
nsv3889882	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 159,815,642-177,026,983 , GRCh38.p12 chr1: 159,845,852-177,057,847	ANKRD45, FMO4, 403 more genes
nsv4346684	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 160,369,890-175,796,325 , GRCh38.p12 chr1: 160,400,100-175,827,189	ANKRD45, LINC00626, 359 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	ANKRD45, CRYZL2P, 233 more genes
nsv3901593	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 161,618,937-174,112,781 , GRCh37 chr1: 163,352,313-175,846,158 , GRCh38 chr1: 163,382,523-175,877,022	ANKRD45, NME7, 233 more genes
nsv3894431	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 159,977,321-172,200,915 , GRCh37 chr1: 161,710,697-173,934,292 , GRCh38 chr1: 161,740,907-173,965,154	ANKRD45, RPL21P27, 238 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	ANKRD45, TRUND-NNN7-1, 210 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	ANKRD45, 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	ANKRD45, 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	ANKRD45, RPS26P12, 150 more genes
nsv3904950	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 166,762,832-175,327,423 , NCBI36 chr1: 164,998,693-173,563,182 , GRCh37 chr1: 166,732,069-175,296,559	ANKRD45, LINC01681, 186 more genes
nsv4674768	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 167,430,471-174,635,618 , GRCh38.p12 chr1: 167,461,234-174,666,480	ANKRD45, ATP1B1, 156 more genes
nsv3893479	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 166,550,684-173,535,058 , GRCh38 chr1: 168,314,822-175,299,299 , GRCh37 chr1: 168,284,060-175,268,435	ANKRD45, GORAB-AS1, 147 more genes
nsv3885421	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 169,095,250-175,778,910 , GRCh38.p12 chr1: 169,126,012-175,809,774	ANKRD45, ZBTB37, 130 more genes
nsv6313519	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757	ANKRD45, RNU6-693P, 73 more genes
nsv6289872	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 173,686,375-176,083,118 , GRCh37.p13 chr1: 173,655,514-176,052,254	ANKRD45, ENTR1P2, 49 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 37

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

Recent activity