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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv7069802inversion1nstd229human GRCh38 chr12: 54,517,308-54,517,341 , GRCh37.p13 chr12: 54,911,092-54,911,125 NCKAP1L
    nsv7063203inversion1nstd229human GRCh38 chr12: 54,524,739-54,524,878 , GRCh37.p13 chr12: 54,918,523-54,918,662 NCKAP1L
    nsv6930628copy number variation1nstd229human GRCh38 chr12: 54,520,741-54,521,446 , GRCh37.p13 chr12: 54,914,525-54,915,230 NCKAP1L
    nsv6924692copy number variation1nstd229human GRCh38 chr12: 54,501,372-54,505,954 , GRCh37.p13 chr12: 54,895,156-54,899,738 NCKAP1L
    nsv6473344copy number variation1nstd223human GRCh38 chr12: 54,523,538-54,524,148 , GRCh37.p13 chr12: 54,917,322-54,917,932 NCKAP1L
    nsv6462273copy number variation1nstd223human GRCh38 chr12: 54,503,861-54,514,601 , GRCh37.p13 chr12: 54,897,645-54,908,385 NCKAP1L
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132426copy number variation1nstd213human GRCh37 chr12: 52,740,000-55,260,001 , GRCh38.p12 chr12: 52,346,216-54,866,217 , HOXC4, 122 more genes
    nsv5135906mobile element insertion1nstd203human GRCh38 chr12: 54,540,185-54,540,202 , GRCh37.p13 chr12: 54,933,969-54,933,986 NCKAP1L
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4972794copy number variation1nstd200human GRCh38 chr12: 54,501,372-54,505,951 , GRCh37.p13 chr12: 54,895,156-54,899,735 NCKAP1L
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 , EIF4B, 163 more genes
    nsv4515646mobile element insertion1nstd166human GRCh37.p13 chr12: 54,923,147-54,923,147 , GRCh38.p12 chr12: 54,529,363-54,529,363 NCKAP1L
    nsv4509865mobile element insertion1nstd166human GRCh37.p13 chr12: 54,937,971-54,937,971 , GRCh38.p12 chr12: 54,544,187-54,544,187 NCKAP1L
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