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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099236copy number variation1nstd231human GRCh38.p12 chr1: 156,064,931-157,804,884 , GRCh37 chr1: 156,034,722-157,774,674 BGLAP, CRABP2, 58 more genes
    nsv7055468inversion1nstd229human GRCh38 chr1: 155,667,181-158,101,472 , GRCh37.p13 chr1: 155,636,972-158,071,262 FCRL4, CRABP2, 88 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
    nsv7039558inversion1nstd229human GRCh38 chr1: 155,298,171-158,468,090 , GRCh37.p13 chr1: 155,267,962-158,437,880 FCRL4, SCARNA4, 121 more genes
    nsv6642547copy number variation1nstd229human GRCh38 chr1: 157,012,726-157,274,163 , GRCh37.p13 chr1: 156,982,518-157,243,953 LOC105371456, ARHGEF11, 8 more genes
    nsv6549694inversion1nstd223human GRCh38 chr1: 155,298,173-158,468,085 , GRCh37.p13 chr1: 155,267,964-158,437,875 ASH1L, GPATCH4, 121 more genes
    nsv6329527copy number variation1nstd223human GRCh38 chr1: 155,481,601-157,146,700 , GRCh37.p13 chr1: 155,451,392-157,116,492 BGLAP, SSR2, 78 more genes
    nsv6324780copy number variation1nstd223human GRCh38 chr1: 157,117,637-157,119,827 , GRCh37.p13 chr1: 157,087,429-157,089,619 ETV3
    nsv6318870copy number variation1nstd223human GRCh38 chr1: 157,126,761-157,127,040 , GRCh37.p13 chr1: 157,096,553-157,096,832 CYCSP52, ETV3
    nsv6151566copy number variation1nstd214human GRCh38 chr1: 157,126,751-157,126,874 , GRCh37.p13 chr1: 157,096,543-157,096,666 CYCSP52, ETV3
    nsv6133588copy number variation1nstd213human GRCh37 chr1: 155,690,000-158,310,001 , GRCh38.p12 chr1: 155,720,209-158,340,211 CD1C, INSRR, 95 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
    nsv6133562copy number variation1nstd213human GRCh37 chr1: 156,040,000-158,340,001 , GRCh38.p12 chr1: 156,070,209-158,370,211 CD1A, CD5L, 75 more genes
    nsv6133561copy number variation1nstd213human GRCh37 chr1: 155,380,000-158,210,001 , GRCh38.p12 chr1: 155,410,209-158,240,211 CD5L, CRABP2, 104 more genes
    nsv5981407copy number variation1nstd212human GRCh38 chr1: 157,126,860-157,126,922 , GRCh37.p13 chr1: 157,096,652-157,096,714 ETV3, CYCSP52
    nsv5694182mobile element insertion2nstd211human GRCh38 chr1: 157,130,782-157,130,782 , GRCh37.p13 chr1: 157,100,574-157,100,574 ETV3
    nsv5418489copy number variation1nstd206human GRCh38 chr1: 157,136,009-157,136,173 , GRCh37.p13 chr1: 157,105,801-157,105,965 ETV3
    nsv5413813mobile element insertion1nstd206human GRCh38 chr1: 157,130,782-157,130,833 , GRCh37.p13 chr1: 157,100,574-157,100,625 ETV3
    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
    nsv5370955translocation1nstd200human GRCh38 chr1: 157,136,108-157,136,108 , GRCh38 chr1: 157,137,027-157,137,027 , GRCh37.p13 chr1: 157,105,900-157,105,900 , GRCh37.p13 chr1: 157,106,819-157,106,819 ETV3
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