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Items: 1 to 20 of 211

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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
    nsv6642641copy number variation1nstd229human GRCh38 chr1: 156,626,610-156,632,896 , GRCh37.p13 chr1: 156,596,402-156,602,688 HAPLN2
    nsv6642640copy number variation1nstd229human GRCh38 chr1: 156,624,808-156,628,142 , GRCh37.p13 chr1: 156,594,600-156,597,934 HAPLN2
    nsv6642314copy number variation1nstd229human GRCh38 chr1: 156,616,201-156,620,179 , GRCh37.p13 chr1: 156,585,993-156,589,971 HAPLN2, LOC101928177
    nsv6553984inversion1nstd223human GRCh38 chr1: 156,613,346-156,614,249 , GRCh37.p13 chr1: 156,583,138-156,584,041 HAPLN2, LOC101928177
    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
    nsv6328622copy number variation1nstd223human GRCh38 chr1: 156,613,128-156,618,501 , GRCh37.p13 chr1: 156,582,920-156,588,293 LOC101928177, HAPLN2
    nsv6319865copy number variation1nstd223human GRCh38 chr1: 156,615,656-156,617,389 , GRCh37.p13 chr1: 156,585,448-156,587,181 HAPLN2, LOC101928177
    nsv6316968copy number variation1nstd223human GRCh38 chr1: 156,611,419-156,613,131 , GRCh37.p13 chr1: 156,581,211-156,582,923 HAPLN2, LOC101928177
    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
    nsv6297412copy number variation1nstd186human GRCh37 chr1: 156,574,709-156,574,835 , GRCh38.p12 chr1: 156,604,917-156,605,043 HAPLN2
    nsv6245296mobile element insertion1nstd215human GRCh38 chr1: 156,623,040-156,623,040 , GRCh37.p13 chr1: 156,592,832-156,592,832 HAPLN2
    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
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