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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6310761copy number variation1nstd102humanPathogenic GRCh37 chr1: 161,137,765-161,138,386 , GRCh38.p12 chr1: 161,167,975-161,168,596 PPOX
    nsv6332500copy number variation1nstd223human GRCh38 chr1: 161,167,633-161,168,731 , GRCh37.p13 chr1: 161,137,423-161,138,521 PPOX
    nsv3131973copy number variation1nstd151human GRCh37 chr1: 161,136,635-161,136,729 , GRCh38.p12 chr1: 161,166,845-161,166,939 PPOX
    esv1459977copy number variation1estd22human NCBI36 chr17: 37,588,996-37,589,004 , GRCh37.p13 chr17: 40,335,470-40,335,478 , GRCh38.p12 chr17: 42,183,452-42,183,460 HCRT
    esv1586808copy number variation1estd22human NCBI36 chr1: 159,403,997-159,403,998 , GRCh37.p13 chr1: 161,137,373-161,137,374 , GRCh38.p12 chr1: 161,167,583-161,167,584 PPOX
    nsv3125086copy number variation1nstd151human GRCh37 chr1: 161,136,887-161,138,978 , GRCh38.p12 chr1: 161,167,097-161,169,188 PPOX
    nsv1873968short tandem repeat7nstd128human GRCh37 chr17: 40,335,431-40,335,478 , GRCh38.p12 chr17: 42,183,413-42,183,460 HCRT
    nsv1872725short tandem repeat1nstd128human GRCh37 chr17: 40,334,333-40,334,373 , GRCh38.p12 chr17: 42,182,315-42,182,355 HCRT
    nsv1873433short tandem repeat6nstd128human GRCh37 chr17: 40,335,494-40,335,531 , GRCh38.p12 chr17: 42,183,476-42,183,513 HCRT
    nsv1873402short tandem repeat1nstd128human GRCh37 chr17: 40,336,501-40,336,522 , GRCh38.p12 chr17: 42,184,483-42,184,504 HCRT
    nsv7144080copy number variation1nstd232human GRCh37.p13 chr1: 161,134,731-161,134,816 , GRCh38.p12 chr1: 161,164,941-161,165,026 PPOX, USP21
    esv3000248copy number variation1estd209human GRCh37 chr1: 161,142,230-161,142,231 , GRCh38.p12 chr1: 161,172,440-161,172,441 PPOX, B4GALT3
    esv3322687copy number variation1estd59human NCBI36 chr1: 159,405,360-159,405,786 , GRCh37.p13 chr1: 161,138,736-161,139,162 , GRCh38.p12 chr1: 161,168,946-161,169,372 PPOX, B4GALT3
    esv1416433copy number variation1estd22human NCBI36 chr1: 159,408,862-159,408,863 , GRCh37.p13 chr1: 161,142,238-161,142,239 , GRCh38.p12 chr1: 161,172,448-161,172,449 PPOX, B4GALT3
    nsv4627701copy number variation1nstd183human GRCh37 chr17: 40,332,923-40,336,459 , GRCh38.p12 chr17: 42,180,905-42,184,441 HCRT, KCNH4
    esv2858370insertion1estd209human GRCh37 chr1: 161,142,473-161,142,473 , GRCh38.p12 chr1: 161,172,683-161,172,683 PPOX, B4GALT3
    esv2444654insertion1estd197human NCBI36 chr1: 159,407,409-159,407,409 , GRCh37.p13 chr1: 161,140,785-161,140,785 , GRCh38.p12 chr1: 161,170,995-161,170,995 PPOX, B4GALT3
    esv2261426insertion1estd194human NCBI36 chr1: 159,409,098-159,409,098 , GRCh37.p13 chr1: 161,142,474-161,142,474 , GRCh38.p12 chr1: 161,172,684-161,172,684 PPOX, B4GALT3
    esv2239612insertion1estd194human NCBI36 chr1: 159,407,410-159,407,410 , GRCh37.p13 chr1: 161,140,786-161,140,786 , GRCh38.p12 chr1: 161,170,996-161,170,996 PPOX, B4GALT3
    esv1496383insertion1estd22human NCBI36 chr1: 159,409,101-159,409,101 , GRCh37.p13 chr1: 161,142,477-161,142,477 , GRCh38.p12 chr1: 161,172,687-161,172,687 PPOX, B4GALT3
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