amotl2[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 17

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Number of Variants: 17

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3920790	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 134,257,180-149,729,538 , NCBI36 chr3: 135,458,712-150,930,015 , GRCh37 chr3: 133,976,022-149,447,325	AMOTL2, TFDP2, 203 more genes
nsv3920279	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 129,817,243-143,381,624 , GRCh37 chr3: 129,536,086-143,100,466 , NCBI36 chr3: 131,018,776-144,583,156	AMOTL2, NPHP3-AS1, 218 more genes
nsv3921297	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 133,918,512-145,986,275 , GRCh38 chr3: 132,716,978-144,784,743 , GRCh37 chr3: 132,435,822-144,503,585	AMOTL2, BFSP2, 169 more genes
nsv3914757	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 131,018,776-142,626,687 , GRCh38 chr3: 129,817,243-141,425,155 , GRCh37 chr3: 129,536,086-141,143,997	AMOTL2, CLSTN2-AS1, 177 more genes
nsv6112714	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 127,927,712-136,889,323 , GRCh38.p12 chr3: 128,208,869-137,170,481	AMOTL2, RNU6-789P, 169 more genes
nsv3918871	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 130,401,265-139,005,019 , NCBI36 chr3: 131,602,799-140,206,551 , GRCh37 chr3: 130,120,109-138,723,861	AMOTL2, FOXL2, 132 more genes
nsv3910942	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr3: 135,535,085-142,902,990 , GRCh38 chr3: 134,333,553-141,701,458 , GRCh37 chr3: 134,052,395-141,420,300	AMOTL2, MRAS, 96 more genes
nsv3920044	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr3: 132,972,567-136,894,498 , GRCh37 chr3: 132,691,411-136,613,340 , NCBI36 chr3: 134,174,101-138,096,030	AMOTL2, TOPBP1, 56 more genes
nsv6634336	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 133,998,370-134,678,040 , GRCh38.p12 chr3: 134,279,528-134,959,198	AMOTL2, MIR6827, 14 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	AMOTL2, 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	AMOTL2, 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	AMOTL2, 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	AMOTL2, LINC02614, 1469 more genes
nsv6637156	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502	AMOTL2, H1-10, 846 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	AMOTL2, OR7E53P, 794 more genes
nsv3872147	copy number variation	1	nstd102	human	Likely pathogenic	GRCh37 chr3: 132,642,704-136,360,844 , GRCh38.p12 chr3: 132,923,860-136,642,002	AMOTL2, EPHB1, 51 more genes
nsv3920834	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr3: 127,308,312-142,119,621 , GRCh38 chr3: 126,106,779-140,918,089 , GRCh37 chr3: 125,825,622-140,636,931	AMOTL2, NCK1-DT, 271 more genes

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amotl2[All Fields] AND 1[has_clinical] (18)
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