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Items: 1 to 20 of 241

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099256copy number variation1nstd231human GRCh38.p12 chr1: 201,916,209-203,311,623 , GRCh37 chr1: 201,885,337-203,280,751 ADORA1, CHI3L1, 49 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv6663516copy number variation1nstd229human GRCh38 chr1: 202,903,113-202,906,409 , GRCh37.p13 chr1: 202,872,241-202,875,537 KLHL12
    nsv6663316copy number variation1nstd229human GRCh38 chr1: 202,886,010-202,889,664 , GRCh37.p13 chr1: 202,855,138-202,858,792 KLHL12, RABIF
    nsv6662283copy number variation1nstd229human GRCh38 chr1: 202,786,930-202,940,996 , GRCh37.p13 chr1: 202,756,058-202,910,124 ACTG1P25, KLHL12, 8 more genes
    nsv6660627copy number variation1nstd229human GRCh38 chr1: 202,586,491-202,889,939 , GRCh37.p13 chr1: 202,555,619-202,859,067 SLC25A39P1, PPP1R12B, 9 more genes
    nsv6659169copy number variation1nstd229human GRCh38 chr1: 202,893,150-202,951,548 , GRCh37.p13 chr1: 202,862,278-202,920,676 HNRNPA1P59, KLHL12, 1 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6555358inversion1nstd223human GRCh38 chr1: 202,902,747-202,903,617 , GRCh37.p13 chr1: 202,871,875-202,872,745 KLHL12
    nsv6548949inversion1nstd223human GRCh38 chr1: 202,920,032-202,920,464 , GRCh37.p13 chr1: 202,889,160-202,889,592 KLHL12
    nsv6543294inversion1nstd223human GRCh38 chr1: 202,906,771-202,907,340 , GRCh37.p13 chr1: 202,875,899-202,876,468 KLHL12
    nsv6538334inversion1nstd223human GRCh38 chr1: 202,928,011-202,928,850 , GRCh37.p13 chr1: 202,897,139-202,897,978 KLHL12
    nsv6538020inversion1nstd223human GRCh38 chr1: 202,916,747-202,917,490 , GRCh37.p13 chr1: 202,885,875-202,886,618 KLHL12
    nsv6326377copy number variation1nstd223human GRCh38 chr1: 202,920,558-202,922,764 , GRCh37.p13 chr1: 202,889,686-202,891,892 KLHL12
    nsv6290683copy number variation1nstd102humanUncertain significance GRCh37 chr1: 202,638,835-202,876,250 , GRCh38.p12 chr1: 202,669,707-202,907,122 MGAT4EP, KDM5B, 8 more genes
    nsv6133960copy number variation1nstd213human GRCh37 chr1: 196,820,000-204,810,001 , GRCh38.p12 chr1: 196,850,870-204,840,873 ELF3, NR5A2, 181 more genes
    nsv6133950copy number variation1nstd213human GRCh37 chr1: 178,070,000-205,920,001 , GRCh38.p12 chr1: 178,100,865-205,950,873 ADORA1, CACNA1E, 442 more genes
    nsv6133842copy number variation1nstd213human GRCh37 chr1: 196,810,000-202,980,001 , GRCh38.p12 chr1: 196,840,870-203,010,873 ELF3, NR5A2, 120 more genes
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