arhgap15[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
nsv3875472	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 144,077,717-144,078,067 , GRCh38.p12 chr2: 143,320,148-143,320,498	ARHGAP15
nsv3879392	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 144,077,823-144,078,170 , GRCh38.p12 chr2: 143,320,254-143,320,601	ARHGAP15
nsv3888995	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 144,077,823-144,078,067 , GRCh38.p12 chr2: 143,320,254-143,320,498	ARHGAP15
nsv3903479	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 144,086,324-144,347,906 , GRCh38 chr2: 143,328,755-143,590,337 , NCBI36 chr2: 143,802,794-144,064,376	ARHGAP15
nsv6636449	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr2: 144,192,888-144,248,006 , GRCh38.p12 chr2: 143,435,319-143,490,437	ARHGAP15
nsv3889165	copy number variation	1	nstd102	human	Benign	GRCh37 chr2: 144,214,631-144,709,343 , GRCh38.p12 chr2: 143,457,062-143,951,776	ARHGAP15, LOC101928361, 3 more genes
nsv3910630	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 50,739,936-242,751,149 , GRCh37.p13 chr2: 50,886,432-243,102,476 , GRCh38.p12 chr2: 50,659,294-242,160,331	ARHGAP15, DAZAP2P1, 2991 more genes
nsv3890186	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 136,937,358-146,681,810 , GRCh37 chr2: 137,694,928-147,439,378 , NCBI36 chr2: 137,411,398-147,155,848	ARHGAP15, SPOPL-DT, 80 more genes
nsv6313481	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 143,258,712-152,867,819 , GRCh38.p12 chr2: 142,501,143-152,011,305	ARHGAP15, STIP1P1, 98 more genes
nsv4685664	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 137,639,637-146,827,604 , GRCh38.p12 chr2: 136,882,067-146,070,036	ARHGAP15, LOC105373651, 75 more genes
nsv3896212	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr2: 140,186,521-146,528,244 , GRCh37 chr2: 140,944,090-147,285,812 , NCBI36 chr2: 140,660,560-147,002,282	ARHGAP15, LOC101928361, 49 more genes
nsv3906959	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr2: 142,140,576-148,319,701 , GRCh38 chr2: 141,666,537-147,845,662 , GRCh37 chr2: 142,424,106-148,603,231	ARHGAP15, MTND6P11, 49 more genes
nsv3909572	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 144,051,648-148,471,399 , NCBI36 chr2: 143,768,118-148,187,869 , GRCh38 chr2: 143,294,079-147,713,830	ARHGAP15, TEX41, 28 more genes
nsv6315390	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305	ARHGAP15, LOC112268439, 3737 more genes
nsv3874648	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 15,672-243,101,834 , GRCh38.p12 chr2: 15,672-242,157,305	ARHGAP15, IGKV2OR2-10, 3737 more genes
nsv3885544	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 14,238-243,048,760 , GRCh38.p12 chr2: 14,238-242,106,609	ARHGAP15, RNU6-674P, 3735 more genes
nsv3882615	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr2: 12,771-242,783,384 , GRCh38.p12 chr2: 12,771-241,841,232	ARHGAP15, MTND2P22, 3724 more genes
nsv6291353	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 111,484,468-146,333,604 , GRCh38.p12 chr2: 110,726,891-145,576,036	ARHGAP15, LINC01120, 490 more genes
nsv6314748	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 112,475,655-145,691,999 , GRCh38.p12 chr2: 111,718,078-144,934,432	ARHGAP15, MED15P9, 474 more genes
nsv5381338	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr2: 136,473,383-152,727,396 , GRCh38.p12 chr2: 135,715,813-151,870,882	ARHGAP15, YY1P2, 156 more genes

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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 30

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Number of Variants: 20

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Supplemental Content

Find related data

Search details

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