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Items: 1 to 20 of 234

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098718copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,206,913-3,771,740 , GRCh38.p12 chr19: 1,206,914-3,771,742 GIPC3, GNG7, 117 more genes
    nsv7095644copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,456,055-2,456,931 , GRCh38.p12 chr19: 1,456,056-2,456,933 APC2, CSNK1G2, 49 more genes
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7073114inversion1nstd229human GRCh38 chr19: 2,143,875-2,402,071 , GRCh37.p13 chr19: 2,143,874-2,402,069 OAZ1, SF3A2, 15 more genes
    nsv7067646inversion1nstd229human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , UHRF1, 192 more genes
    nsv7016706copy number variation1nstd229human GRCh38 chr19: 2,129,001-2,344,100 , GRCh37.p13 chr19: 2,129,000-2,344,098 AP3D1, MIR4321, 14 more genes
    nsv7014793copy number variation1nstd229human GRCh38 chr19: 2,298,995-2,299,590 , GRCh37.p13 chr19: 2,298,994-2,299,589 LINGO3
    nsv7008526copy number variation1nstd229human GRCh38 chr19: 2,298,779-2,299,388 , GRCh37.p13 chr19: 2,298,778-2,299,387 LINGO3
    nsv7007182copy number variation1nstd229human GRCh38 chr19: 2,296,754-2,311,042 , GRCh37.p13 chr19: 2,296,753-2,311,041 LINGO3, LOC101928572
    nsv7006672copy number variation1nstd229human GRCh38 chr19: 2,290,101-2,291,400 , GRCh37.p13 chr19: 2,290,100-2,291,399 LINGO3
    nsv7006285copy number variation1nstd229human GRCh38 chr19: 2,301,063-2,303,072 , GRCh37.p13 chr19: 2,301,062-2,303,071 LINGO3, LOC101928572
    nsv7005690copy number variation1nstd229human GRCh38 chr19: 2,276,293-2,308,236 , GRCh37.p13 chr19: 2,276,292-2,308,235 LOC101928572, PEAK3, 1 more genes
    nsv6597296inversion1nstd223human GRCh38 chr19: 2,282,380-7,636,598 , GRCh37.p13 chr19: 2,282,379-7,701,484 , ALKBH7, 192 more genes
    nsv6534123copy number variation1nstd223human GRCh38 chr19: 2,299,461-2,299,761 , GRCh37.p13 chr19: 2,299,460-2,299,760 LINGO3
    nsv6525465copy number variation1nstd223human GRCh38 chr19: 2,293,482-2,297,985 , GRCh37.p13 chr19: 2,293,481-2,297,984 LINGO3
    nsv6521867copy number variation1nstd223human GRCh38 chr19: 2,298,392-2,299,673 , GRCh37.p13 chr19: 2,298,391-2,299,672 LINGO3
    nsv6291606copy number variation1nstd102humanUncertain significance GRCh37 chr19: 1,973,753-2,380,699 , GRCh38.p12 chr19: 1,973,754-2,380,701 DOT1L, LOC107985278, 20 more genes
    nsv6242742mobile element insertion1nstd215human GRCh38 chr19: 2,289,882-2,289,882 , GRCh37.p13 chr19: 2,289,881-2,289,881 LINGO3
    nsv6133468copy number variation1nstd213human GRCh37 chr19: 2,040,000-7,300,001 , GRCh38.p12 chr19: 2,040,001-7,299,990 TLE5, AMH, 192 more genes
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