dppa2[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
nsv7148201	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 93,979,547-124,774,010 , GRCh37.p13 chr3: 93,698,391-124,492,857	DPPA2, NECTIN3, 418 more genes
nsv3918661	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683	DPPA2, MTCO2P29, 401 more genes
nsv3917160	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,021,157-118,088,593 , GRCh38 chr3: 93,819,623-116,887,056 , GRCh37 chr3: 93,538,467-116,605,903	DPPA2, ATP6V1A, 297 more genes
nsv3910775	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 97,514,213-115,382,196 , GRCh38 chr3: 97,795,369-115,663,349 , NCBI36 chr3: 98,996,903-116,864,886	DPPA2, ZBTB11-AS1, 258 more genes
nsv3911662	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 102,633,427-117,731,277 , GRCh37.p13 chr3: 101,150,737-116,248,587 , GRCh38.p12 chr3: 101,431,893-116,529,740	DPPA2, SIDT1, 188 more genes
nsv3888585	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 105,094,834-117,441,953 , GRCh38.p12 chr3: 105,375,990-117,723,106	DPPA2, RFKP2, 165 more genes
nsv4674254	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 101,812,245-112,174,485 , GRCh38.p12 chr3: 102,093,401-112,455,638	DPPA2, IFT57, 111 more genes
nsv6315408	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 106,598,767-115,704,696 , GRCh38.p12 chr3: 106,879,920-115,985,849	DPPA2, DZIP3, 138 more genes
nsv6636830	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 107,059,705-115,005,256 , GRCh38.p12 chr3: 107,340,858-115,286,409	DPPA2, ATP6V1A, 117 more genes
nsv3913048	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 109,444,109-117,370,868 , GRCh38 chr3: 108,242,572-116,169,331 , GRCh37 chr3: 107,961,419-115,888,178	DPPA2, RPSAP29, 115 more genes
nsv3913722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,411,064-109,324,749 , GRCh38 chr3: 103,692,220-109,605,902 , NCBI36 chr3: 104,893,754-110,807,439	DPPA2, MTND4P16, 64 more genes
nsv3885606	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156	DPPA2, RNU4-62P, 2880 more genes
nsv3889228	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115	DPPA2, NDUFB4, 2876 more genes
nsv3880617	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 61,495-197,838,262 , GRCh38.p12 chr3: 19,817-198,111,391	DPPA2, RPL23AP49, 2875 more genes
nsv3918981	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446	DPPA2, LINC02614, 1469 more genes
nsv3922717	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168	DPPA2, OR7E53P, 794 more genes
nsv3913319	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 105,822,754-117,295,421 , GRCh38 chr3: 104,621,220-116,093,884 , GRCh37 chr3: 104,340,064-115,812,731	DPPA2, TAGLN3, 151 more genes
nsv3886411	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 108,597,544-109,019,701 , GRCh38.p12 chr3: 108,878,697-109,300,854	DPPA2, GUCA1C, 6 more genes
nsv3871860	copy number variation	1	nstd102	human	Likely benign	GRCh37 chr3: 108,616,806-109,014,594 , GRCh38.p12 chr3: 108,897,959-109,295,747	DPPA2, RNU6-1236P, 6 more genes
nsv3910754	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 110,503,479-111,003,709 , GRCh37.p13 chr3: 109,020,789-109,521,019 , GRCh38.p12 chr3: 109,301,942-109,802,172	DPPA2, DPPA4, 6 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 21

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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