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Items: 1 to 20 of 129

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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
    nsv6642649copy number variation1nstd229human GRCh38 chr1: 156,805,020-156,809,699 , GRCh37.p13 chr1: 156,774,812-156,779,491 SH2D2A
    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
    nsv6316639copy number variation1nstd223human GRCh38 chr1: 156,809,771-156,810,911 , GRCh37.p13 chr1: 156,779,563-156,780,703 SH2D2A
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6310593copy number variation1nstd102humanPathogenic GRCh37 chr1: 155,581,953-156,851,434 , GRCh38.p12 chr1: 155,612,162-156,881,642 MIR9-1, MRPL24, 62 more genes
    nsv6310523copy number variation1nstd102humanUncertain significance GRCh37 chr1: 154,141,761-156,851,434 , GRCh38.p12 chr1: 154,169,285-156,881,642 MIR555, CFAP141, 135 more genes
    nsv6297476copy number variation1nstd186human GRCh37 chr1: 156,774,812-156,779,491 , GRCh38.p12 chr1: 156,805,020-156,809,699 SH2D2A
    nsv6290596copy number variation1nstd102humanUncertain significance GRCh37 chr1: 156,665,257-156,902,706 , GRCh38.p12 chr1: 156,695,465-156,932,914 ISG20L2, PEAR1, 10 more genes
    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
    nsv5961200insertion1nstd209human GRCh38 chr1: 156,817,047-156,817,047 , GRCh37.p13 chr1: 156,786,839-156,786,839 NTRK1, SH2D2A
    nsv5430187copy number variation1nstd206human GRCh38 chr1: 156,805,020-156,809,699 , GRCh37.p13 chr1: 156,774,812-156,779,491 SH2D2A
    nsv5414546copy number variation1nstd206human GRCh38 chr1: 156,809,771-156,810,911 , GRCh37.p13 chr1: 156,779,563-156,780,703 SH2D2A
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