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Items: 1 to 20 of 606

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5963563insertion1nstd209human GRCh38 chr2: 188,298,290-188,298,290 , GRCh37.p13 chr2: 189,163,017-189,163,017 GULP1
    nsv5900781copy number variation1nstd209human GRCh38 chr2: 188,411,911-188,413,459 , GRCh37.p13 chr2: 189,276,638-189,278,186 GULP1
    nsv5887833copy number variation1nstd209human GRCh38 chr2: 188,587,435-188,594,600 , GRCh37.p13 chr2: 189,452,162-189,459,327 GULP1
    nsv5831808copy number variation1nstd209human GRCh38 chr2: 188,587,412-188,594,611 , GRCh37.p13 chr2: 189,452,139-189,459,338 GULP1
    nsv5693751mobile element insertion2nstd211human GRCh38 chr2: 188,451,894-188,451,894 , GRCh37.p13 chr2: 189,316,621-189,316,621 GULP1
    nsv5691020mobile element insertion1nstd211human GRCh38 chr2: 188,450,484-188,450,484 , GRCh37.p13 chr2: 189,315,211-189,315,211 GULP1
    nsv5688731mobile element insertion1nstd211human GRCh38 chr2: 188,471,510-188,471,510 , GRCh37.p13 chr2: 189,336,237-189,336,237 GULP1
    nsv5687702mobile element insertion2nstd211human GRCh38 chr2: 188,439,242-188,439,242 , GRCh37.p13 chr2: 189,303,969-189,303,969 GULP1
    nsv5686432mobile element insertion2nstd211human GRCh38 chr2: 188,298,290-188,298,290 , GRCh37.p13 chr2: 189,163,017-189,163,017 GULP1
    nsv5682703mobile element insertion2nstd211human GRCh38 chr2: 188,345,032-188,345,032 , GRCh37.p13 chr2: 189,209,759-189,209,759 GULP1
    nsv5682255mobile element insertion2nstd211human GRCh38 chr2: 188,343,316-188,343,316 , GRCh37.p13 chr2: 189,208,043-189,208,043 GULP1
    nsv5620625insertion1nstd207human GRCh38 chr2: 188,298,290-188,298,290 , GRCh37.p13 chr2: 189,163,017-189,163,017 GULP1
    nsv5605738insertion1nstd207human GRCh38 chr2: 188,345,018-188,345,018 , GRCh37.p13 chr2: 189,209,745-189,209,745 GULP1
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5550405insertion1nstd206human GRCh38 chr2: 188,298,290-188,298,290 , GRCh37.p13 chr2: 189,163,017-189,163,017 GULP1
    nsv5452619copy number variation1nstd206human GRCh38 chr2: 188,495,641-188,496,003 , GRCh37.p13 chr2: 189,360,368-189,360,730 GULP1
    nsv5452614copy number variation1nstd206human GRCh38 chr2: 188,481,137-188,482,885 , GRCh37.p13 chr2: 189,345,864-189,347,612 GULP1
    nsv5450092copy number variation1nstd206human GRCh38 chr2: 188,410,338-188,411,388 , GRCh37.p13 chr2: 189,275,065-189,276,115 GULP1
    nsv5448757copy number variation1nstd206human GRCh38 chr2: 188,547,440-188,547,864 , GRCh37.p13 chr2: 189,412,167-189,412,591 GULP1
    nsv5441524copy number variation1nstd206human GRCh38 chr2: 188,360,454-188,364,319 , GRCh37.p13 chr2: 189,225,181-189,229,046 GULP1
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