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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096308copy number variation1nstd102humanUncertain significance GRCh37 chr22: 35,776,672-42,486,826 , GRCh38.p12 chr22: 35,380,679-42,090,822 CDC42EP1, SREBF2, 231 more genes
    nsv7077764inversion1nstd229human GRCh38 chr22: 37,971,370-41,589,449 , GRCh37.p13 chr22: 38,367,377-41,985,453 UQCRFS1P1, LOC105373027, 119 more genes
    nsv7062036inversion1nstd229human GRCh38 chr22: 41,220,102-41,224,933 , GRCh37.p13 chr22: 41,616,106-41,620,937 L3MBTL2
    nsv7061959inversion1nstd229human GRCh38 chr22: 36,818,005-44,993,640 , GRCh37.p13 chr22: 37,214,049-45,389,520 SMIM45, A4GALT, 271 more genes
    nsv7058666inversion1nstd229human GRCh38 chr22: 39,066,437-42,707,681 , GRCh37.p13 chr22: 39,462,442-43,103,687 LOC101927344, ATF4, 128 more genes
    nsv7030153copy number variation1nstd229human GRCh38 chr22: 41,228,735-41,247,128 , GRCh37.p13 chr22: 41,624,739-41,643,132 L3MBTL2, RANGAP1, 1 more genes
    nsv7029911copy number variation1nstd229human GRCh38 chr22: 41,184,501-41,252,200 , GRCh37.p13 chr22: 41,580,505-41,648,204 LOC646927, L3MBTL2-AS1, 6 more genes
    nsv7029110copy number variation1nstd229human GRCh38 chr22: 41,227,203-41,234,947 , GRCh37.p13 chr22: 41,623,207-41,630,951 L3MBTL2, CHADL
    nsv7027741copy number variation1nstd229human GRCh38 chr22: 39,432,386-49,047,389 , GRCh37.p13 chr22: 39,828,391-49,443,201 LOC105373064, ACO2, 233 more genes
    nsv7027241copy number variation1nstd229human GRCh38 chr22: 41,206,235-41,210,576 , GRCh37.p13 chr22: 41,602,239-41,606,580 L3MBTL2, L3MBTL2-AS1
    nsv7023981copy number variation1nstd229human GRCh38 chr22: 41,189,421-41,219,319 , GRCh37.p13 chr22: 41,585,425-41,615,323 LOC646927, EP300-AS1, 3 more genes
    nsv7023840copy number variation1nstd229human GRCh38 chr22: 41,198,635-41,204,235 , GRCh37.p13 chr22: 41,594,639-41,600,239 L3MBTL2
    nsv7023452copy number variation1nstd229human GRCh38 chr22: 41,183,197-41,231,815 , GRCh37.p13 chr22: 41,579,201-41,627,819 LOC646927, L3MBTL2, 4 more genes
    nsv7022955copy number variation1nstd229human GRCh38 chr22: 41,175,146-41,333,607 , GRCh37.p13 chr22: 41,571,150-41,729,611 EP300, MIR6889, 8 more genes
    nsv7021854copy number variation1nstd229human GRCh38 chr22: 41,203,940-41,204,211 , GRCh37.p13 chr22: 41,599,944-41,600,215 L3MBTL2
    nsv6637214copy number variation1nstd102humanUncertain significance GRCh37 chr22: 39,768,795-41,946,225 , GRCh38.p12 chr22: 39,372,790-41,550,221 MRTFA-AS1, LOC105373043, 62 more genes
    nsv6596534inversion1nstd223human GRCh38 chr22: 39,133,553-42,757,193 , GRCh37.p13 chr22: 39,529,558-43,153,199 POLR3H, ACO2, 123 more genes
    nsv6552653copy number variation1nstd223human GRCh38 chr22: 41,210,424-41,211,701 , GRCh37.p13 chr22: 41,606,428-41,607,705 L3MBTL2, L3MBTL2-AS1
    nsv6550804copy number variation1nstd223human GRCh38 chr22: 41,183,197-41,231,810 , GRCh37.p13 chr22: 41,579,201-41,627,814 L3MBTL2-AS1, EP300-AS1, 4 more genes
    nsv6548168copy number variation1nstd223human GRCh38 chr22: 41,185,740-41,210,105 , GRCh37.p13 chr22: 41,581,744-41,606,109 LOC646927, EP300-AS1, 3 more genes
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