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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980068inversion1nstd209human GRCh38 chr1: 204,546,577-204,562,849 , GRCh37.p13 chr1: 204,515,705-204,531,977 MDM4, RNA5SP74, 1 more genes
    nsv5829094copy number variation1nstd209human GRCh38 chr1: 204,543,536-204,546,035 , GRCh37.p13 chr1: 204,512,664-204,515,163 MDM4
    nsv5829002copy number variation1nstd209human GRCh38 chr1: 204,552,081-204,562,282 , GRCh37.p13 chr1: 204,521,209-204,531,410 RNA5SP74, LOC105371692, 1 more genes
    nsv5829001copy number variation1nstd209human GRCh38 chr1: 204,506,441-204,521,719 , GRCh37.p13 chr1: 204,475,569-204,490,847 MDM4, TRK-TTT3-2, 1 more genes
    nsv5610525insertion1nstd207human GRCh38 chr1: 204,515,830-204,515,830 , GRCh37.p13 chr1: 204,484,958-204,484,958 MDM4
    nsv5450743copy number variation1nstd206human GRCh38 chr1: 204,544,950-204,545,002 , GRCh37.p13 chr1: 204,514,078-204,514,130 MDM4
    nsv5381285copy number variation2nstd102humanUncertain significance GRCh37 chr1: 130,980,840-248,900,000 , GRCh38.p12 chr1: 120,324,463-248,736,699 , DCST1, 2428 more genes
    nsv5216086mobile element deletion1nstd204human GRCh38.p13 chr1: 204,539,989-204,540,310 , GRCh37.p13 chr1: 204,509,117-204,509,438 MDM4
    nsv5078696mobile element insertion1nstd203human GRCh38 chr1: 204,515,830-204,515,846 , GRCh37.p13 chr1: 204,484,958-204,484,974 MDM4
    nsv4891683copy number variation1nstd200human GRCh38 chr1: 204,555,222-204,557,412 , GRCh37.p13 chr1: 204,524,350-204,526,540 MDM4
    nsv4891682copy number variation1nstd200human GRCh38 chr1: 204,539,192-204,541,328 , GRCh37.p13 chr1: 204,508,320-204,510,456 MDM4
    nsv4789317copy number variation1nstd200human GRCh37 chr1: 204,524,350-204,526,540 , GRCh38.p12 chr1: 204,555,222-204,557,412 MDM4
    nsv4774104mobile element deletion1nstd200human GRCh37 chr1: 204,509,126-204,509,430 , GRCh38.p12 chr1: 204,539,998-204,540,302 MDM4
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4685577copy number variation1nstd102humannot provided GRCh37 chr1: 194,356,425-210,988,710 , GRCh38.p12 chr1: 194,387,295-210,815,368 SEPTIN14P12, LINC02602, 332 more genes
    nsv4674140copy number variation1nstd102humanPathogenic GRCh37 chr1: 204,045,948-249,218,992 , GRCh38.p12 chr1: 204,076,820-248,924,793 RNA5S8, NTPCR, 893 more genes
    nsv4580350copy number variation1nstd183human GRCh37 chr1: 204,512,265-204,515,299 , GRCh38.p12 chr1: 204,543,137-204,546,171 MDM4
    nsv4450583copy number variation1nstd102humanPathogenic GRCh37 chr1: 182,388,773-249,111,240 , GRCh38.p12 chr1: 182,419,638-248,817,041 RGS18, LINC02257, 1186 more genes
    nsv4057924copy number variation1nstd166human GRCh37.p13 chr1: 204,484,360-204,484,492 , GRCh38.p12 chr1: 204,515,232-204,515,364 MDM4
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