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Items: 1 to 20 of 147

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6993404copy number variation1nstd229human GRCh38 chr17: 78,168,717-78,170,815 , GRCh37.p13 chr17: 76,164,798-76,166,896 SYNGR2
    nsv6522158copy number variation1nstd223human GRCh38 chr17: 78,170,417-78,170,701 , GRCh37.p13 chr17: 76,166,498-76,166,782 SYNGR2
    nsv5530798copy number variation1nstd206human GRCh38 chr17: 78,167,662-78,167,987 , GRCh37.p13 chr17: 76,163,743-76,164,068 SYNGR2
    nsv6523113copy number variation1nstd223human GRCh38 chr17: 78,167,017-78,167,834 , GRCh37.p13 chr17: 76,163,098-76,163,915 SYNGR2
    nsv5552677insertion1nstd206human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv6131053insertion1nstd186human GRCh37 chr17: 76,163,788-76,163,788 , GRCh38.p12 chr17: 78,167,707-78,167,707 SYNGR2
    nsv5155861mobile element insertion1nstd203human GRCh38 chr17: 78,167,552-78,167,588 , GRCh37.p13 chr17: 76,163,633-76,163,669 SYNGR2
    nsv5148597mobile element insertion1nstd203human GRCh38 chr17: 78,167,706-78,167,719 , GRCh37.p13 chr17: 76,163,787-76,163,800 SYNGR2
    nsv5149880mobile element insertion1nstd203human GRCh38 chr17: 78,167,707-78,167,719 , GRCh37.p13 chr17: 76,163,788-76,163,800 SYNGR2
    nsv5662993insertion1nstd207human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    nsv5979945insertion1nstd209human GRCh38 chr17: 78,167,707-78,167,707 , GRCh37.p13 chr17: 76,163,788-76,163,788 SYNGR2
    esv2420556insertion1estd194human NCBI36 chr17: 73,676,963-73,676,963 , GRCh37.p13 chr17: 76,165,368-76,165,368 , GRCh38.p12 chr17: 78,169,287-78,169,287 SYNGR2
    nsv1897710short tandem repeat5nstd128human GRCh37 chr17: 76,163,466-76,163,505 , GRCh38.p12 chr17: 78,167,385-78,167,424 SYNGR2
    nsv1897711short tandem repeat1nstd128human GRCh37 chr17: 76,164,669-76,164,695 , GRCh38.p12 chr17: 78,168,588-78,168,614 SYNGR2
    nsv1897709short tandem repeat3nstd128human GRCh37 chr17: 76,163,017-76,163,036 , GRCh38.p12 chr17: 78,166,936-78,166,955 SYNGR2
    nsv1897712short tandem repeat9nstd128human GRCh37 chr17: 76,165,338-76,165,355 , GRCh38.p12 chr17: 78,169,257-78,169,274 SYNGR2
    nsv6995824copy number variation1nstd229human GRCh38 chr17: 78,164,380-78,168,026 , GRCh37.p13 chr17: 76,160,461-76,164,107 SYNGR2, C17orf99
    nsv6996134copy number variation1nstd229human GRCh38 chr17: 78,170,920-78,172,600 , GRCh37.p13 chr17: 76,167,001-76,168,681 SYNGR2, TK1
    esv3796117complex chromosomal rearrangement2estd192human GRCh37 chr15: 34,027,741-34,027,761 , GRCh37 chr17: 76,165,442-76,165,462 , GRCh38.p12 chr17: 78,169,361-78,169,381 , GRCh38.p12 chr15: 33,735,540-33,735,560 SYNGR2, RYR3
    nsv6994801copy number variation1nstd229human GRCh38 chr17: 78,157,486-78,174,492 , GRCh37.p13 chr17: 76,153,567-76,170,573 SYNGR2, TK1, 2 more genes
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