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Items: 1 to 20 of 161

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980026insertion1nstd209human GRCh38 chr14: 76,793,391-76,793,391 , GRCh37.p13 chr14: 77,259,734-77,259,734 ANGEL1
    nsv5936743copy number variation1nstd209human GRCh38 chr14: 76,808,435-76,808,526 , GRCh37.p13 chr14: 77,274,778-77,274,869 ANGEL1
    nsv5931678copy number variation1nstd209human GRCh38 chr14: 75,925,125-77,416,814 , GRCh37.p13 chr14: 76,391,468-77,883,157 TMED8, LOC105370573, 37 more genes
    nsv5729289mobile element insertion2nstd211human GRCh38 chr14: 76,794,688-76,794,688 , GRCh37.p13 chr14: 77,261,031-77,261,031 ANGEL1
    nsv5664269insertion1nstd207human GRCh38 chr14: 76,793,391-76,793,391 , GRCh37.p13 chr14: 77,259,734-77,259,734 ANGEL1
    nsv5647950insertion1nstd207human GRCh38 chr14: 76,793,369-76,793,369 , GRCh37.p13 chr14: 77,259,712-77,259,712 ANGEL1
    nsv5593355copy number variation1nstd207human GRCh38 chr14: 76,808,435-76,808,526 , GRCh37.p13 chr14: 77,274,778-77,274,869 ANGEL1
    nsv5496372copy number variation1nstd206human GRCh38 chr14: 76,808,436-76,808,527 , GRCh37.p13 chr14: 77,274,779-77,274,870 ANGEL1
    nsv5357413translocation1nstd200human GRCh38 chr14: 76,808,527-76,808,527 , GRCh38 chr14: 76,808,436-76,808,436 , GRCh37.p13 chr14: 77,274,779-77,274,779 , GRCh37.p13 chr14: 77,274,870-77,274,870 ANGEL1
    nsv5357410translocation1nstd200human GRCh38 chr14: 76,658,034-76,658,034 , GRCh38 chr14: 76,811,612-76,811,612 , GRCh37.p13 chr14: 77,277,955-77,277,955 , GRCh37.p13 chr14: 77,124,377-77,124,377 ANGEL1
    nsv5275249copy number variation1nstd204human GRCh38.p13 chr14: 76,789,901-76,798,900 , GRCh37.p13 chr14: 77,256,244-77,265,243 ANGEL1
    nsv5195099mobile element insertion1nstd203human GRCh38 chr14: 76,796,637-76,796,651 , GRCh37.p13 chr14: 77,262,980-77,262,994 ANGEL1
    nsv5192326mobile element insertion1nstd203human GRCh38 chr14: 76,794,674-76,794,688 , GRCh37.p13 chr14: 77,261,017-77,261,031 ANGEL1
    nsv5189349mobile element insertion1nstd203human GRCh38 chr14: 76,794,670-76,794,688 , GRCh37.p13 chr14: 77,261,013-77,261,031 ANGEL1
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5004816copy number variation1nstd200human GRCh38 chr14: 76,494,566-76,823,810 , GRCh37.p13 chr14: 76,960,909-77,290,153 ESRRB, CYCSP1, 7 more genes
    nsv4751956insertion1nstd199human GRCh37 chr14: 77,259,711-77,259,711 , GRCh38.p12 chr14: 76,793,368-76,793,368 ANGEL1
    nsv4654914copy number variation1nstd186human GRCh37 chr14: 77,274,779-77,274,870 , GRCh38.p12 chr14: 76,808,436-76,808,527 ANGEL1
    nsv4577298mobile element insertion1nstd166human GRCh37.p13 chr14: 77,262,980-77,262,980 , GRCh38.p12 chr14: 76,796,637-76,796,637 ANGEL1
    nsv4576539mobile element insertion1nstd166human GRCh37.p13 chr14: 77,262,342-77,262,342 , GRCh38.p12 chr14: 76,795,999-76,795,999 ANGEL1
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