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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057183inversion1nstd229human GRCh38 chr7: 21,972,222-23,503,741 , GRCh37.p13 chr7: 22,011,840-23,543,360 TRA2A, IGF2BP3, 30 more genes
    nsv7042850inversion1nstd229human GRCh38 chr7: 22,833,698-23,236,044 , GRCh37.p13 chr7: 22,873,317-23,275,663 LOC105375185, KLHL7-DT, 11 more genes
    nsv7042193inversion1nstd229human GRCh38 chr7: 23,162,006-23,606,884 , GRCh37.p13 chr7: 23,201,625-23,646,503 NUP42, RPS2P32, 13 more genes
    nsv6809538copy number variation1nstd229human GRCh38 chr7: 23,192,683-23,213,041 , GRCh37.p13 chr7: 23,232,302-23,252,660 NUP42, LOC101927890
    nsv6809395copy number variation1nstd229human GRCh38 chr7: 23,165,943-23,244,625 , GRCh37.p13 chr7: 23,205,562-23,284,244 LOC101927890, NUP42, 1 more genes
    nsv6805181copy number variation1nstd229human GRCh38 chr7: 23,187,001-23,190,800 , GRCh37.p13 chr7: 23,226,620-23,230,419 NUP42
    nsv6803301copy number variation1nstd229human GRCh38 chr7: 23,179,316-23,181,402 , GRCh37.p13 chr7: 23,218,935-23,221,021 NUP42
    nsv6802762copy number variation1nstd229human GRCh38 chr7: 23,177,915-23,181,399 , GRCh37.p13 chr7: 23,217,534-23,221,018 NUP42, KLHL7
    nsv6801800copy number variation1nstd229human GRCh38 chr7: 23,186,101-23,464,800 , GRCh37.p13 chr7: 23,225,720-23,504,419 IGF2BP3, LOC101927890, 5 more genes
    nsv6799756copy number variation1nstd229human GRCh38 chr7: 23,129,075-23,242,744 , GRCh37.p13 chr7: 23,168,694-23,282,363 AK3P3, NUP42, 2 more genes
    nsv6798714copy number variation1nstd229human GRCh38 chr7: 23,191,346-23,193,152 , GRCh37.p13 chr7: 23,230,965-23,232,771 NUP42
    nsv6636524copy number variation1nstd102humanUncertain significance GRCh37 chr7: 22,949,862-23,470,342 , GRCh38.p12 chr7: 22,910,243-23,430,723 KLHL7-DT, AK3P3, 10 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631688copy number variation1nstd224human GRCh37 chr7: 23,226,691-23,240,353 , GRCh38.p12 chr7: 23,187,072-23,200,734 NUP42
    nsv6631686copy number variation1nstd224human GRCh37 chr7: 22,712,877-23,240,353 , GRCh38.p12 chr7: 22,673,258-23,200,734 TOMM7, RPS26P32, 15 more genes
    nsv6619149copy number variation1nstd223human GRCh38 chr7: 23,177,922-23,181,350 , GRCh37.p13 chr7: 23,217,541-23,220,969 KLHL7, NUP42
    nsv6610287copy number variation1nstd223human GRCh38 chr7: 23,175,322-23,188,985 , GRCh37.p13 chr7: 23,214,941-23,228,604 NUP42, KLHL7
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313493copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 10,745,750-35,305,167 , GRCh38.p12 chr7: 10,706,123-35,265,556 ADCYAP1R1, AHR, 329 more genes
    nsv6135913copy number variation1nstd213human GRCh37 chr7: 23,090,000-24,440,001 , GRCh38.p12 chr7: 23,050,381-24,400,382 GPNMB, IGF2BP3, 25 more genes
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