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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3184998copy number variation1estd209human GRCh37 chr14: 75,543,464-75,543,468 , GRCh38.p12 chr14: 75,076,761-75,076,765 ZC2HC1C
    esv2577240copy number variation1estd197human NCBI36 chr14: 74,613,218-74,613,221 , GRCh37.p13 chr14: 75,543,465-75,543,468 , GRCh38.p12 chr14: 75,076,762-75,076,765 ZC2HC1C
    esv2354524copy number variation1estd194human NCBI36 chr14: 74,613,218-74,613,222 , GRCh37.p13 chr14: 75,543,465-75,543,469 , GRCh38.p12 chr14: 75,076,762-75,076,766 ZC2HC1C
    esv1357307copy number variation1estd22human NCBI36 chr14: 74,613,218-74,613,222 , GRCh37.p13 chr14: 75,543,465-75,543,469 , GRCh38.p12 chr14: 75,076,762-75,076,766 ZC2HC1C
    nsv1772932short tandem repeat2nstd128human GRCh37 chr14: 75,542,764-75,542,801 , GRCh38.p12 chr14: 75,076,061-75,076,098 ZC2HC1C
    nsv1751090short tandem repeat3nstd128human GRCh37 chr14: 75,541,267-75,541,297 , GRCh38.p12 chr14: 75,074,564-75,074,594 ZC2HC1C
    nsv1751890short tandem repeat1nstd128human GRCh37 chr14: 75,542,966-75,542,986 , GRCh38.p12 chr14: 75,076,263-75,076,283 ZC2HC1C
    nsv6962263copy number variation1nstd229human GRCh38 chr14: 75,055,992-75,068,202 , GRCh37.p13 chr14: 75,522,695-75,534,905 ZC2HC1C, ACYP1
    nsv6969713copy number variation1nstd229human GRCh38 chr14: 75,062,186-75,070,714 , GRCh37.p13 chr14: 75,528,889-75,537,417 ZC2HC1C, ACYP1
    nsv6972684copy number variation1nstd229human GRCh38 chr14: 75,077,370-75,079,727 , GRCh37.p13 chr14: 75,544,073-75,546,430 ZC2HC1C, NEK9
    nsv6485364copy number variation1nstd223human GRCh38 chr14: 75,055,983-75,068,201 , GRCh37.p13 chr14: 75,522,686-75,534,904 ZC2HC1C, ACYP1
    nsv5000084copy number variation1nstd200human GRCh38 chr14: 75,077,370-75,079,727 , GRCh37.p13 chr14: 75,544,073-75,546,430 ZC2HC1C, NEK9
    nsv4838048copy number variation1nstd200human GRCh37 chr14: 75,544,073-75,546,430 , GRCh38.p12 chr14: 75,077,370-75,079,727 ZC2HC1C, NEK9
    esv3184999copy number variation1estd209human GRCh37 chr14: 75,547,043-75,547,049 , GRCh38.p12 chr14: 75,080,340-75,080,346 ZC2HC1C, NEK9
    esv1631198copy number variation1estd22human NCBI36 chr14: 74,615,690-74,615,691 , GRCh37.p13 chr14: 75,545,937-75,545,938 , GRCh38.p12 chr14: 75,079,234-75,079,235 ZC2HC1C, NEK9
    nsv3093605mobile element insertion1nstd144human GRCh37 chr14: 75,535,425-75,535,425 , GRCh38.p12 chr14: 75,068,722-75,068,722 ZC2HC1C, ACYP1
    esv2322129insertion1estd194human NCBI36 chr14: 74,605,169-74,605,169 , GRCh37.p13 chr14: 75,535,416-75,535,416 , GRCh38.p12 chr14: 75,068,713-75,068,713 ZC2HC1C, ACYP1
    nsv6588941inversion1nstd223human GRCh38 chr14: 75,080,130-75,080,677 , GRCh37.p13 chr14: 75,546,833-75,547,380 ZC2HC1C, NEK9
    nsv1751089short tandem repeat1nstd128human GRCh37 chr14: 75,535,040-75,535,068 , GRCh38.p12 chr14: 75,068,337-75,068,365 ZC2HC1C, ACYP1
    nsv1772933short tandem repeat8nstd128human GRCh37 chr14: 75,547,032-75,547,057 , GRCh38.p12 chr14: 75,080,329-75,080,354 ZC2HC1C, NEK9
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