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Items: 1 to 20 of 79

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3901564copy number variation1nstd102humanBenign GRCh37 chr17: 2,393,319-2,402,480 , GRCh38.p12 chr17: 2,490,025-2,499,186 METTL16
    nsv3896149copy number variation1nstd102humanBenign GRCh37 chr17: 2,399,614-2,402,378 , GRCh38.p12 chr17: 2,496,320-2,499,084 METTL16
    nsv3906642copy number variation1nstd102humanLikely benign GRCh37 chr17: 2,316,530-2,475,180 , GRCh38.p12 chr17: 2,413,236-2,571,886 METTL16, LOC284009, 1 more genes
    nsv3892349copy number variation1nstd102humanUncertain significance GRCh37 chr17: 2,336,350-2,548,911 , GRCh38.p12 chr17: 2,433,056-2,645,617 METTL16, EIF4A1P9, 3 more genes
    nsv3913076copy number variation1nstd102humanUncertain significance GRCh37 chr17: 2,393,729-2,542,161 , NCBI36 chr17: 2,340,479-2,488,911 , GRCh38 chr17: 2,490,435-2,638,867 METTL16, SAMD11P1, 3 more genes
    nsv3913339copy number variation1nstd102humanUncertain significance GRCh38 chr17: 2,473,511-2,594,380 , NCBI36 chr17: 2,323,555-2,444,424 , GRCh37 chr17: 2,376,805-2,497,674 METTL16, EIF4A1P9, 2 more genes
    nsv3913013copy number variation1nstd102humanPathogenic GRCh38 chr17: 162,016-7,697,012 , GRCh37 chr17: 45,835-7,600,330 , NCBI36 chr17: 11,807-7,541,055 METTL16, RPS4XP17, 289 more genes
    nsv3915884copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-6,862,369 , GRCh38 chr17: 162,088-6,959,050 , NCBI36 chr17: 11,879-6,803,093 METTL16, LOC105371592, 222 more genes
    nsv3922546copy number variation1nstd102humanPathogenic NCBI36 chr17: 525-5,779,421 , GRCh38 chr17: 150,732-5,935,377 , GRCh37 chr17: 525-5,838,697 METTL16, CHRNE, 198 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 METTL16, SRR, 196 more genes
    nsv3913795copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,098-5,496,266 , GRCh37 chr17: 45,835-5,555,542 , GRCh38 chr17: 193,307-5,652,222 METTL16, BHLHA9, 194 more genes
    nsv3921779copy number variation1nstd102humanPathogenic NCBI36 chr17: 87,039-4,585,577 , GRCh38 chr17: 237,248-4,735,533 , GRCh37 chr17: 396,627-4,638,828 METTL16, ARRB2, 146 more genes
    nsv3919819copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-4,168,935 , NCBI36 chr17: 48,539-4,115,684 , GRCh38 chr17: 198,748-4,265,640 METTL16, LOC105371430, 125 more genes
    nsv3904699copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-3,871,323 , GRCh38.p12 chr17: 157,423-3,968,029 METTL16, OVCA2, 120 more genes
    nsv3892866copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-3,825,428 , GRCh38.p12 chr17: 150,732-3,922,134 METTL16, OR1P1, 120 more genes
    nsv3920266copy number variation1nstd102humanPathogenic GRCh38 chr17: 226,472-3,655,099 , NCBI36 chr17: 76,263-3,505,142 , GRCh37 chr17: 396,627-3,558,393 METTL16, RN7SL624P, 107 more genes
    nsv3902288copy number variation1nstd102humanPathogenic GRCh37 chr17: 48,858-3,379,400 , GRCh38.p12 chr17: 199,067-3,476,106 METTL16, GEMIN4, 100 more genes
    nsv3920795copy number variation1nstd102humanPathogenic GRCh38 chr17: 2,062,380-5,258,340 , NCBI36 chr17: 1,912,424-5,102,359 , GRCh37 chr17: 1,965,674-5,161,635 METTL16, LINC01996, 128 more genes
    nsv3913766copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-3,242,868 , NCBI36 chr17: 525-3,092,912 , GRCh37 chr17: 525-3,146,162 METTL16, LOC105371483, 90 more genes
    nsv3919726copy number variation1nstd102humanPathogenic GRCh37 chr17: 50,690-3,005,626 , NCBI36 chr17: 48,539-2,952,376 , GRCh38 chr17: 198,748-3,102,332 METTL16, RN7SL608P, 81 more genes
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