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Items: 1 to 20 of 3736

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137719copy number variation1nstd102humanLikely benign GRCh38 chr15: 100,887,321-100,887,380 , GRCh37 chr15: 101,427,526-101,427,585 ALDH1A3
    nsv6129211insertion1nstd186human GRCh37 chr12: 122,319,733-122,319,763 , GRCh38.p12 chr12: 121,881,827-121,881,857 HPD
    nsv6122488copy number variation1nstd186human GRCh37 chr12: 103,320,594-103,320,829 , GRCh38.p12 chr12: 102,926,816-102,927,051 PAH, LOC112267865
    nsv6120695copy number variation1nstd186human GRCh37 chr12: 122,282,572-122,283,380 , GRCh38.p12 chr12: 121,844,666-121,845,474 HPD
    nsv6115561copy number variation1nstd186human GRCh37 chrX: 43,669,208-43,669,515 , GRCh38.p12 chrX: 43,809,961-43,810,268 MAOB
    nsv6112780copy number variation1nstd102humanPathogenic GRCh37 chr15: 92,335,751-102,399,741 , GRCh38.p12 chr15: 91,792,521-101,859,538 LOC105371009, ST8SIA2, 149 more genes
    nsv6112722copy number variation1nstd102humanPathogenic GRCh37 chrX: 42,069,104-45,843,277 , GRCh38.p12 chrX: 42,209,851-45,983,842 TATDN2P1, RRM2P3, 36 more genes
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5978803insertion1nstd209human GRCh38 chr12: 121,881,827-121,881,827 , GRCh37.p13 chr12: 122,319,733-122,319,733 HPD
    nsv5978267insertion1nstd209human GRCh38 chr17: 42,848,525-42,848,525 , GRCh37.p13 chr17: 41,000,542-41,000,542 AOC2
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5973346inversion1nstd209human GRCh38 chr12: 118,054,601-123,705,841 , GRCh37.p13 chr12: 118,492,406-124,190,388 , ACADS, 162 more genes
    nsv5973246inversion1nstd209human GRCh38 chr15: 97,535,582-101,746,493 , GRCh37.p13 chr15: 98,078,812-102,286,696 , ALDH1A3, 71 more genes
    nsv5968000inversion1nstd209human GRCh38 chr22: 23,676,272-24,601,321 , GRCh37.p13 chr22: 24,018,459-24,997,288 , ADORA2A, 38 more genes
    nsv5958899copy number variation1nstd209human GRCh38 chr22: 22,653,852-24,634,860 , GRCh37.p13 chr22: 22,996,322-25,030,827 , LOC105372957, 122 more genes
    nsv5956621copy number variation1nstd209human GRCh38 chr22: 22,621,614-24,637,144 , GRCh37.p13 chr22: 22,964,084-25,033,111 , IGLV2-5, 125 more genes
    nsv5947048copy number variation1nstd209human GRCh38 chr12: 102,916,503-102,931,394 , GRCh37.p13 chr12: 103,310,281-103,325,172 LOC112267865, PAH
    nsv5940810copy number variation1nstd209human GRCh38 chr12: 102,835,644-102,835,793 , GRCh37.p13 chr12: 103,229,422-103,229,571 PAH
    nsv5940439copy number variation1nstd209human GRCh38 chr12: 102,848,267-102,848,371 , GRCh37.p13 chr12: 103,242,045-103,242,149 PAH
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