vwa1[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
nsv3875938	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 1,374,436-1,431,285 , GRCh38.p12 chr1: 1,439,056-1,495,905	VWA1, ATAD3B, 1 more genes
nsv3887855	copy number variation	1	nstd102	human	Benign	GRCh37 chr1: 1,377,437-1,431,285 , GRCh38.p12 chr1: 1,442,057-1,495,905	VWA1, ATAD3C, 1 more genes
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	VWA1, RPL9P11, 466 more genes
nsv3873030	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 746,608-15,077,159 , GRCh38.p12 chr1: 811,228-14,750,663	VWA1, RN7SL451P, 376 more genes
nsv3888433	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-12,699,337 , GRCh38.p12 chr1: 82,154-12,639,316	VWA1, AURKAIP1, 356 more genes
nsv4436105	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-11,784,118 , GRCh38.p12 chr1: 82,154-11,724,061	VWA1, PARK7, 325 more genes
nsv3899046	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 844,347-12,470,133 , GRCh37 chr1: 779,727-12,530,188 , NCBI36 chr1: 769,590-12,452,775	VWA1, PRKCZ-DT, 315 more genes
nsv6637093	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897	VWA1, CEP104, 311 more genes
nsv6315409	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-10,258,804 , GRCh38.p12 chr1: 914,086-10,198,746	VWA1, VAMP3, 245 more genes
nsv4436631	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 554,375-9,779,842 , GRCh38.p12 chr1: 618,995-9,719,784	VWA1, LINC02606, 253 more genes
nsv3913374	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 4,737-8,767,973 , GRCh37.p13 chr1: 14,874-8,845,386 , GRCh38.p12 chr1: 14,874-8,785,327	VWA1, LOC105378593, 252 more genes
nsv3907841	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 837,491-9,616,363 , GRCh38 chr1: 902,111-9,556,305 , NCBI36 chr1: 827,354-9,538,950	VWA1, PRKCZ-AS1, 224 more genes
nsv3890178	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 839,329-9,549,767 , GRCh37 chr1: 849,466-9,627,180 , GRCh38 chr1: 914,086-9,567,122	VWA1, ANKRD65, 224 more genes
nsv3909850	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 846,680-9,389,984 , GRCh38 chr1: 911,300-9,329,925 , NCBI36 chr1: 836,543-9,312,571	VWA1, LOC105378590, 221 more genes
nsv3889222	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-8,901,938 , GRCh38.p12 chr1: 914,086-8,841,879	VWA1, PLEKHG5, 205 more genes
nsv3894118	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 554,268-8,520,391 , GRCh38 chr1: 629,025-8,537,745 , GRCh37 chr1: 564,405-8,597,804	VWA1, TNFRSF14, 223 more genes
nsv3898457	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 859,215-8,747,647 , GRCh37 chr1: 794,595-8,807,706 , NCBI36 chr1: 784,458-8,730,293	VWA1, NOC2L, 205 more genes
nsv3885153	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-7,936,272 , GRCh38.p12 chr1: 82,154-7,876,212	VWA1, TTLL10-AS1, 226 more genes
nsv4435992	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 82,154-7,637,060 , GRCh38.p12 chr1: 82,154-7,577,000	VWA1, SNORD167, 222 more genes
nsv3924689	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 4,737-7,449,889 , GRCh37.p13 chr1: 14,874-7,527,302 , GRCh38.p12 chr1: 14,874-7,467,242	VWA1, MIR6726, 230 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 155

Page of 8

Number of Variants: 20

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Supplemental Content

Find related data

Search details

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