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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099238copy number variation1nstd231human GRCh38.p12 chr1: 158,547,193-159,184,138 , GRCh37 chr1: 158,516,983-159,153,928 IFI16, MNDA, 23 more genes
    nsv7046668inversion1nstd229human GRCh38 chr1: 158,867,577-159,867,183 , GRCh37.p13 chr1: 158,837,367-159,836,973 PYHIN1, ACKR1, 35 more genes
    nsv7041047inversion1nstd229human GRCh38 chr1: 154,596,558-159,585,927 , GRCh37.p13 chr1: 154,569,034-159,555,717 ADAR, SNORA80E, 204 more genes
    nsv6643302copy number variation1nstd229human GRCh38 chr1: 159,168,231-159,177,042 , GRCh37.p13 chr1: 159,138,021-159,146,832 RNA5SP60, CADM3
    nsv6642974copy number variation1nstd229human GRCh38 chr1: 159,156,578-160,055,287 , GRCh37.p13 chr1: 159,126,368-160,025,077 RPL27AP2, ACKR1, 38 more genes
    nsv6320390copy number variation1nstd223human GRCh38 chr1: 159,186,250-159,186,612 , GRCh37.p13 chr1: 159,156,040-159,156,402 CADM3
    nsv6310595copy number variation2nstd102humanUncertain significance GRCh37 chr1: 158,581,054-162,750,036 , GRCh38.p12 chr1: 158,611,264-162,780,246 IGSF8, SETP9, 193 more genes
    nsv6290655copy number variation1nstd102humanUncertain significance GRCh37 chr1: 158,822,741-159,244,974 , GRCh38.p12 chr1: 158,852,951-159,275,184 PYDC5, CADM3-AS1, 10 more genes
    nsv6133742copy number variation1nstd213human GRCh37 chr1: 158,430,000-161,510,001 , GRCh38.p12 chr1: 158,460,210-161,540,211 APCS, FCER1A, 174 more genes
    nsv6133741copy number variation1nstd213human GRCh37 chr1: 158,390,000-161,480,001 , GRCh38.p12 chr1: 158,420,210-161,510,211 ATP1A4, CD48, 169 more genes
    nsv6133740copy number variation1nstd213human GRCh37 chr1: 158,330,000-161,530,001 , GRCh38.p12 chr1: 158,360,210-161,560,211 ATP1A2, ATP1A4, 178 more genes
    nsv6133563copy number variation1nstd213human GRCh37 chr1: 156,490,000-159,480,001 , GRCh38.p12 chr1: 156,520,208-159,510,211 CD1A, CD1D, 104 more genes
    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
    nsv4903949copy number variation1nstd200human GRCh38 chr1: 159,160,217-159,183,899 , GRCh37.p13 chr1: 159,130,007-159,153,689 CADM3, RNA5SP60
    nsv4903948copy number variation1nstd200human GRCh38 chr1: 159,156,577-160,055,289 , GRCh37.p13 chr1: 159,126,367-160,025,079 , IGSF9, 40 more genes
    nsv4784418copy number variation1nstd200human GRCh37 chr1: 159,156,041-159,156,402 , GRCh38.p12 chr1: 159,186,251-159,186,612 CADM3
    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
    nsv4450412copy number variation1nstd102humanPathogenic GRCh37 chr1: 157,321,299-167,391,423 , GRCh38.p12 chr1: 157,351,509-167,422,186 FCGR3B, SLAMF9, 302 more genes
    nsv4385444copy number variation1nstd173human GRCh37 chr1: 158,214,469-159,706,408 , GRCh38.p12 chr1: 158,244,679-159,736,618 , RAD1P2, 60 more genes
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