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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3150380copy number variation1nstd151human GRCh37 (hg19) chr15: 48,717,563-48,755,442 , GRCh38 (hg38) chr15: 48,425,366-48,463,245 FBN1
    nsv3149146copy number variation1nstd151human GRCh37 (hg19) chr15: 48,707,730-49,083,578 , GRCh38 (hg38) chr15: 48,415,533-48,791,381 FBN1, CEP152
    nsv3148080copy number variation1nstd151human GRCh37 (hg19) chr15: 48,826,274-49,034,302 , GRCh38 (hg38) chr15: 48,534,077-48,742,105 FBN1, CEP152
    nsv3147759copy number variation1nstd151human GRCh37 (hg19) chr15: 48,740,962-48,802,371 , GRCh38 (hg38) chr15: 48,448,765-48,510,174 FBN1
    nsv3147645copy number variation1nstd151human GRCh37 (hg19) chr15: 48,713,752-48,726,915 , GRCh38 (hg38) chr15: 48,421,555-48,434,718 FBN1
    nsv3147297copy number variation1nstd151human GRCh37 (hg19) chr15: 48,764,745-48,780,443 , GRCh38 (hg38) chr15: 48,472,548-48,488,246 FBN1
    nsv3144611copy number variation1nstd151human GRCh37 (hg19) chr15: 48,712,881-48,720,673 , GRCh38 (hg38) chr15: 48,420,684-48,428,476 FBN1
    nsv3143788copy number variation1nstd151human GRCh37 (hg19) chr15: 48,737,570-48,936,971 , GRCh38 (hg38) chr15: 48,445,373-48,644,774 FBN1
    nsv3140104copy number variation1nstd151human GRCh37 (hg19) chr15: 48,719,761-48,755,442 , GRCh38 (hg38) chr15: 48,427,564-48,463,245 FBN1
    nsv3099980mobile element insertion1nstd144human GRCh37 (hg19) chr15: 48,812,831-48,812,831 , GRCh38 (hg38) chr15: 48,520,634-48,520,634 FBN1
    nsv3095748mobile element insertion1nstd144human GRCh37 (hg19) chr15: 48,740,421-48,740,421 , GRCh38 (hg38) chr15: 48,448,224-48,448,224 FBN1
    nsv3094773mobile element insertion1nstd144human GRCh37 (hg19) chr15: 48,926,692-48,926,692 , GRCh38 (hg38) chr15: 48,634,495-48,634,495 FBN1
    nsv2779140copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 21,173,967-100,338,915 , GRCh37 (hg19) chr15: 23,622,526-102,521,392 , GRCh38 (hg38) chr15: 23,377,379-101,981,189 NR2E3, SNORD116-1, 882 more genes
    nsv2778543copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 18,323,354-100,338,915 , GRCh37 (hg19) chr15: 20,063,340-102,521,392 , GRCh38 (hg38) chr15: 19,858,087-101,981,189 NR2E3, SNORD116-1, 913 more genes
    nsv2777964copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr15: 48,771,569-48,892,364 , GRCh38 (hg38) chr15: 48,479,372-48,600,167 , NCBI36 (hg18) chr15: 46,558,861-46,679,656 FBN1
    nsv2777568copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 41,689,327-52,446,981 , GRCh38 (hg38) chr15: 41,397,129-52,154,784 , NCBI36 (hg18) chr15: 39,476,619-50,234,273 MIR147B, GABPB1-AS1, 132 more genes
    nsv2777189copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr15: 26,996,912-100,338,915 , GRCh37 (hg19) chr15: 29,209,620-102,521,392 , GRCh38 (hg38) chr15: 28,917,417-101,981,189 NR2E3, FAM138E, 757 more genes
    nsv2776267copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr15: 20,733,395-102,511,616 , GRCh38 (hg38) chr15: 20,528,156-101,971,413 , NCBI36 (hg18) chr15: 18,993,409-100,329,139 NR2E3, SNORD116-1, 908 more genes
    nsv2775831copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr15: 22,770,422-102,429,112 , GRCh38 (hg38) chr15: 22,358,243-101,888,909 , NCBI36 (hg18) chr15: 20,321,786-100,246,635 NR2E3, SNORD116-1, 886 more genes
    nsv2775394copy number variation1nstd37humanUncertain significance GRCh37 (hg19) chr15: 48,606,170-48,732,716 , GRCh38 (hg38) chr15: 48,313,973-48,440,519 , NCBI36 (hg18) chr15: 46,393,462-46,520,008 DUT, FBN1
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