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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094366copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,526,072-35,087,019 , GRCh38.p12 chr15: 34,233,871-34,794,818 NUTM1, ACTC1, 16 more genes
    nsv7071130inversion1nstd229human GRCh38 chr15: 33,339,608-35,270,089 , GRCh37.p13 chr15: 33,631,809-35,562,290 LOC105370765, AQR, 38 more genes
    nsv7063469inversion1nstd229human GRCh38 chr15: 33,686,568-35,388,285 , GRCh37.p13 chr15: 33,978,769-35,680,486 NUTM1, AVEN, 41 more genes
    nsv6968887copy number variation1nstd229human GRCh38 chr15: 34,401,701-34,549,900 , GRCh37.p13 chr15: 34,693,902-34,842,101 HNRNPLP2, MIR1233-2, 5 more genes
    nsv6967555copy number variation1nstd229human GRCh38 chr15: 34,431,311-34,431,344 , GRCh37.p13 chr15: 34,723,512-34,723,545 GOLGA8A
    nsv6634442copy number variation1nstd102humanPathogenic GRCh37 chr15: 32,915,722-34,671,601 , GRCh38.p12 chr15: 32,623,521-34,379,400 KATNBL1, ARHGAP11A, 27 more genes
    nsv6623248copy number variation2nstd224human GRCh37 chr15: 34,666,301-34,967,574 , GRCh38.p12 chr15: 34,374,100-34,675,373 FSCN1P1, GOLGA8B, 9 more genes
    nsv6623247copy number variation1nstd224human GRCh37 chr15: 34,655,021-34,967,574 , GRCh38.p12 chr15: 34,362,820-34,675,373 FSCN1P1, LPCAT4, 10 more genes
    nsv6623246copy number variation1nstd224human GRCh37 chr15: 34,651,912-34,967,574 , GRCh38.p12 chr15: 34,359,711-34,675,373 FSCN1P1, LPCAT4, 10 more genes
    nsv6623106copy number variation1nstd224human GRCh37 chr15: 34,666,149-34,982,488 , GRCh38.p12 chr15: 34,373,948-34,690,287 HNRNPLP2, ACTG1P15, 9 more genes
    nsv6623079copy number variation1nstd224human GRCh37 chr15: 34,724,487-35,036,386 , GRCh38.p12 chr15: 34,432,286-34,744,185 GOLGA8A, FSCN1P1, 6 more genes
    nsv6623078copy number variation4nstd224human GRCh37 chr15: 34,724,487-34,761,123 , GRCh38.p12 chr15: 34,432,286-34,468,922 GOLGA8A
    nsv6623077copy number variation1nstd224human GRCh37 chr15: 34,722,783-34,761,123 , GRCh38.p12 chr15: 34,430,582-34,468,922 GOLGA8A
    nsv6622888copy number variation8nstd224human GRCh37 chr15: 34,722,783-34,982,488 , GRCh38.p12 chr15: 34,430,582-34,690,287 GOLGA8A, FSCN1P1, 6 more genes
    nsv6622887copy number variation7nstd224human GRCh37 chr15: 34,719,098-34,761,123 , GRCh38.p12 chr15: 34,426,897-34,468,922 GOLGA8A
    nsv6514763copy number variation1nstd223human GRCh38 chr15: 34,431,327-34,577,496 , GRCh37.p13 chr15: 34,723,528-34,869,697 GOLGA8B, FSCN1P1, 5 more genes
    nsv6514076copy number variation1nstd223human GRCh38 chr15: 34,418,501-34,438,000 , GRCh37.p13 chr15: 34,710,702-34,730,201 GOLGA8A
    nsv6514054copy number variation1nstd223human GRCh38 chr15: 34,423,001-34,437,100 , GRCh37.p13 chr15: 34,715,202-34,729,301 GOLGA8A
    nsv6513948copy number variation1nstd223human GRCh38 chr15: 34,435,601-34,437,400 , GRCh37.p13 chr15: 34,727,802-34,729,601 GOLGA8A
    nsv6513015copy number variation1nstd223human GRCh38 chr15: 34,438,101-34,488,900 , GRCh37.p13 chr15: 34,730,302-34,781,101 HNRNPLP2, GOLGA8A
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