ctnnbip1[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
nsv6290672	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 849,466-17,525,065 , GRCh38.p12 chr1: 914,086-17,198,570	CTNNBIP1, RPL9P11, 466 more genes
nsv7098827	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749	CTNNBIP1, LOC107985467, 386 more genes
nsv3900501	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 3,006,193-17,688,934 , GRCh37 chr1: 2,922,757-18,015,429 , NCBI36 chr1: 2,912,617-17,888,016	CTNNBIP1, MFFP1, 364 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	CTNNBIP1, RN7SL451P, 376 more genes
nsv3900236	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 5,363,826-18,360,302 , GRCh37 chr1: 5,423,886-18,686,796 , NCBI36 chr1: 5,323,746-18,559,383	CTNNBIP1, PDPN, 333 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	CTNNBIP1, AURKAIP1, 356 more genes
nsv6636785	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276	CTNNBIP1, GPR157, 313 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	CTNNBIP1, 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	CTNNBIP1, 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	CTNNBIP1, VWA1, 311 more genes
nsv3905483	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 6,303,641-15,799,093 , NCBI36 chr1: 6,286,288-15,998,175 , GRCh37 chr1: 6,363,701-16,125,588	CTNNBIP1, VPS13D, 240 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	CTNNBIP1, VAMP3, 245 more genes
nsv3885408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,558,588-13,187,457 , GRCh38.p12 chr1: 4,498,528-13,119,984	CTNNBIP1, PRAMEF2, 198 more genes
nsv3903444	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 4,958,499-13,178,528 , NCBI36 chr1: 4,858,359-13,101,115 , GRCh38 chr1: 4,898,439-13,111,056	CTNNBIP1, NPPA-AS1, 195 more genes
nsv3896270	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 4,898,439-12,911,913 , NCBI36 chr1: 4,858,359-12,894,344 , GRCh37 chr1: 4,958,499-12,971,757	CTNNBIP1, LINC01647, 185 more genes
nsv3897535	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 9,017,317-16,640,547 , GRCh38 chr1: 9,034,671-16,441,465 , GRCh37 chr1: 9,094,730-16,767,960	CTNNBIP1, RNU6-771P, 206 more genes
nsv3891889	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 9,428,538-15,815,791 , NCBI36 chr1: 9,411,184-16,014,873 , GRCh37 chr1: 9,488,597-16,142,286	CTNNBIP1, PRAMEF31P, 178 more genes
nsv3891532	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr1: 7,147,683-13,101,115 , GRCh37 chr1: 7,225,096-13,178,528 , GRCh38 chr1: 7,165,036-13,111,056	CTNNBIP1, RNU6ATAC18P, 159 more genes
nsv3903387	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr1: 8,343,754-12,530,188 , GRCh38 chr1: 8,283,694-12,470,133 , NCBI36 chr1: 8,266,341-12,452,775	CTNNBIP1, TNFRSF1B, 113 more genes
nsv3903672	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr1: 9,064,492-12,666,744 , NCBI36 chr1: 9,047,138-12,649,342 , GRCh37 chr1: 9,124,551-12,726,755	CTNNBIP1, LOC105376712, 101 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 38

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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