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Items: 1 to 20 of 141

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5874151copy number variation1nstd209human GRCh38 chr1: 13,714,112-20,623,728 , GRCh37.p13 chr1: 14,040,607-20,950,221 , TRV-CAC11-1, 171 more genes
    nsv5868577copy number variation1nstd209human GRCh38 chr1: 15,581,636-15,582,029 , GRCh37.p13 chr1: 15,908,131-15,908,524 AGMAT
    nsv5828251copy number variation1nstd209human GRCh38 chr1: 15,572,311-15,578,854 , GRCh37.p13 chr1: 15,898,806-15,905,349 DNAJC16, AGMAT
    nsv5213403copy number variation1nstd204human GRCh37.p13 chr1: 15,803,496-15,937,395 , GRCh38.p13 chr1: 15,477,001-15,610,900 CASP9, CD24P1, 6 more genes
    nsv5066801mobile element insertion1nstd203human GRCh38 chr1: 15,576,767-15,576,813 , GRCh37.p13 chr1: 15,903,262-15,903,308 AGMAT
    nsv4903105copy number variation1nstd200human GRCh38 chr1: 15,562,734-15,585,389 , GRCh37.p13 chr1: 15,889,229-15,911,884 DNAJC16, AGMAT
    nsv4895001copy number variation1nstd200human GRCh38 chr1: 15,582,209-15,585,984 , GRCh37.p13 chr1: 15,908,704-15,912,479 AGMAT
    nsv4895000copy number variation1nstd200human GRCh38 chr1: 15,581,748-15,591,331 , GRCh37.p13 chr1: 15,908,243-15,917,826 AGMAT
    nsv4894999copy number variation1nstd200human GRCh38 chr1: 15,580,749-15,591,231 , GRCh37.p13 chr1: 15,907,244-15,917,726 AGMAT
    nsv4783096copy number variation1nstd200human GRCh37 chr1: 15,908,243-15,917,826 , GRCh38.p12 chr1: 15,581,748-15,591,331 AGMAT
    nsv4783095copy number variation1nstd200human GRCh37 chr1: 15,907,244-15,917,725 , GRCh38.p12 chr1: 15,580,749-15,591,230 AGMAT
    nsv4772185copy number variation1nstd200human GRCh37 chr1: 15,889,229-15,911,884 , GRCh38.p12 chr1: 15,562,734-15,585,389 AGMAT, DNAJC16
    nsv4567950mobile element insertion1nstd166human GRCh37.p13 chr1: 15,896,681-15,896,681 , GRCh38.p12 chr1: 15,570,186-15,570,186 AGMAT, DNAJC16
    nsv4436680complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-24,379,779 , GRCh37 chr1: 909,238-24,706,269 ALPL, RERE, 636 more genes
    nsv4436526complex substitution1nstd102humanUncertain significance GRCh38.p12 chr1: 973,858-16,409,637 , GRCh37 chr1: 909,238-16,736,132 RERE, CA6, 415 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4049065copy number variation1nstd166human GRCh37.p13 chr1: 15,888,097-15,964,416 , GRCh38.p12 chr1: 15,561,602-15,637,921 CD24P1, DNAJC16, 4 more genes
    nsv4040520copy number variation1nstd166human GRCh37.p13 chr1: 15,908,240-15,917,848 , GRCh38.p12 chr1: 15,581,745-15,591,353 AGMAT
    nsv4039486copy number variation1nstd166human GRCh37.p13 chr1: 15,907,204-15,917,724 , GRCh38.p12 chr1: 15,580,709-15,591,229 AGMAT
    nsv3970667copy number variation1nstd168human GRCh38 chr1: 15,578,896-15,615,460 , GRCh37.p13 chr1: 15,905,391-15,941,955 DDI2, CHCHD2P6, 3 more genes
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