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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099193copy number variation1nstd231human GRCh38.p12 chr1: 32,456,017-38,905,781 , GRCh37 chr1: 32,921,618-39,371,453 AK2, COL8A2, 151 more genes
    nsv7046918inversion1nstd229human GRCh38 chr1: 34,689,928-38,980,899 , GRCh37.p13 chr1: 35,155,529-39,446,571 LOC105378647, NCDN, 112 more genes
    nsv7040332inversion1nstd229human GRCh38 chr1: 34,936,903-38,057,517 , GRCh37.p13 chr1: 35,402,504-38,523,189 MAP7D1, RPL12P45, 83 more genes
    nsv6649563copy number variation1nstd229human GRCh38 chr1: 37,509,005-37,559,946 , GRCh37.p13 chr1: 37,974,606-38,025,547 SNIP1, RPS27P9, 4 more genes
    nsv6649507copy number variation1nstd229human GRCh38 chr1: 37,489,310-37,514,748 , GRCh37.p13 chr1: 37,954,911-37,980,349 MEAF6, MIR5581
    nsv6649506copy number variation1nstd229human GRCh38 chr1: 37,486,470-37,489,291 , GRCh37.p13 chr1: 37,952,071-37,954,892 MEAF6
    nsv6553342inversion1nstd223human GRCh38 chr1: 37,502,760-37,503,570 , GRCh37.p13 chr1: 37,968,361-37,969,171 MEAF6
    nsv6553126inversion1nstd223human GRCh38 chr1: 37,504,609-37,505,173 , GRCh37.p13 chr1: 37,970,210-37,970,774 MEAF6
    nsv6550597inversion1nstd223human GRCh38 chr1: 37,502,321-37,503,365 , GRCh37.p13 chr1: 37,967,922-37,968,966 MEAF6
    nsv6541036inversion1nstd223human GRCh38 chr1: 37,498,553-37,499,046 , GRCh37.p13 chr1: 37,964,154-37,964,647 MIR5581, MEAF6
    nsv6540736inversion1nstd223human GRCh38 chr1: 37,491,301-37,492,198 , GRCh37.p13 chr1: 37,956,902-37,957,799 MEAF6
    nsv6331866copy number variation1nstd223human GRCh38 chr1: 37,507,754-37,544,375 , GRCh37.p13 chr1: 37,973,355-38,009,976 SNIP1, LOC105378649, 2 more genes
    nsv6313765copy number variation1nstd102humanUncertain significance GRCh37 chr1: 36,041,366-39,112,237 , GRCh38.p12 chr1: 35,575,765-38,646,565 RNU6-510P, AGO3, 78 more genes
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6133994copy number variation1nstd213human GRCh37 chr1: 37,480,000-43,930,001 , GRCh38.p12 chr1: 37,014,399-43,464,330 BMP8B, CDC20, 183 more genes
    nsv5874325copy number variation1nstd209human GRCh38 chr1: 37,494,447-37,494,762 , GRCh37.p13 chr1: 37,960,048-37,960,363 MEAF6
    nsv5674577mobile element insertion1nstd211human GRCh38 chr1: 37,492,581-37,492,581 , GRCh37.p13 chr1: 37,958,182-37,958,182 MEAF6
    nsv5424733copy number variation1nstd206human GRCh38 chr1: 37,514,809-37,514,859 , GRCh37.p13 chr1: 37,980,410-37,980,460 MEAF6
    nsv5197323mobile element insertion1nstd203human GRCh38 chr1: 37,506,273-37,506,273 , GRCh37.p13 chr1: 37,971,874-37,971,874 MEAF6
    nsv5078459mobile element insertion1nstd203human GRCh38 chr1: 37,513,150-37,513,165 , GRCh37.p13 chr1: 37,978,751-37,978,766 MEAF6
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