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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6994222copy number variation1nstd229human GRCh38 chr17: 75,628,476-75,637,042 , GRCh37.p13 chr17: 73,624,556-73,633,122 SMIM5, RECQL5
    nsv6984412copy number variation1nstd229human GRCh38 chr17: 75,631,600-75,631,643 , GRCh37.p13 chr17: 73,627,680-73,627,723 SMIM5, RECQL5
    nsv3166667copy number variation2nstd151human GRCh37 chr17: 73,623,499-73,627,753 , GRCh38.p12 chr17: 75,627,419-75,631,673 SMIM5, RECQL5
    esv2953128insertion1estd209human GRCh37 chr17: 73,628,442-73,628,442 , GRCh38.p12 chr17: 75,632,362-75,632,362 SMIM5, RECQL5
    esv2439171insertion1estd197human NCBI36 chr17: 71,145,865-71,145,865 , GRCh37.p13 chr17: 73,634,270-73,634,270 , GRCh38.p12 chr17: 75,638,190-75,638,190 SMIM5, RECQL5
    esv2120246insertion1estd194human NCBI36 chr17: 71,145,860-71,145,860 , GRCh37.p13 chr17: 73,634,265-73,634,265 , GRCh38.p12 chr17: 75,638,185-75,638,185 SMIM5, RECQL5
    nsv1898050short tandem repeat2nstd128human GRCh37 chr17: 73,629,953-73,629,979 , GRCh38.p12 chr17: 75,633,873-75,633,899 SMIM5, RECQL5
    esv3776263complex chromosomal rearrangement1estd192human GRCh37 chr17: 73,631,473-73,631,493 , GRCh37 chr20: 43,329,555-43,329,575 , GRCh38.p12 chr17: 75,635,393-75,635,413 , GRCh38.p12 chr20: 44,700,914-44,700,934 SMIM5, RECQL5
    nsv3890986copy number variation1nstd102humanBenign GRCh37 chr17: 73,517,536-73,627,539 , GRCh38.p12 chr17: 75,521,455-75,631,459 SMIM5, RECQL5, 3 more genes
    nsv3898320copy number variation1nstd102humanBenign GRCh37 chr17: 73,600,891-73,641,899 , GRCh38.p12 chr17: 75,604,810-75,645,819 SMIM5, MYO15B, 2 more genes
    nsv3897042copy number variation1nstd102humanBenign GRCh37 chr17: 73,600,891-73,627,539 , GRCh38.p12 chr17: 75,604,810-75,631,459 SMIM5, RECQL5, 1 more genes
    nsv3908580copy number variation1nstd102humanBenign GRCh37 chr17: 73,606,275-73,627,539 , GRCh38.p12 chr17: 75,610,194-75,631,459 SMIM5, MYO15B, 1 more genes
    nsv6520781copy number variation1nstd223human GRCh38 chr17: 75,577,126-75,638,253 , GRCh37.p13 chr17: 73,573,207-73,634,333 SMIM5, MYO15B, 1 more genes
    nsv2787550copy number variation1nstd132human NCBI36 chr17: 71,070,937-71,153,309 , GRCh37.p13 chr17: 73,559,342-73,641,714 , GRCh38.p12 chr17: 75,563,261-75,645,634 SMIM5, MYO15B, 3 more genes
    nsv2782142copy number variation1nstd132human NCBI36 chr17: 71,065,523-71,139,134 , GRCh37.p13 chr17: 73,553,928-73,627,539 , GRCh38.p12 chr17: 75,557,847-75,631,459 SMIM5, RECQL5, 2 more genes
    nsv2783951copy number variation1nstd132human NCBI36 chr17: 71,070,937-71,139,134 , GRCh37.p13 chr17: 73,559,342-73,627,539 , GRCh38.p12 chr17: 75,563,261-75,631,459 SMIM5, RECQL5, 2 more genes
    nsv2787985copy number variation1nstd132human NCBI36 chr17: 71,097,953-71,139,134 , GRCh37.p13 chr17: 73,586,358-73,627,539 , GRCh38.p12 chr17: 75,590,277-75,631,459 SMIM5, MYO15B, 1 more genes
    nsv2785744copy number variation1nstd132human NCBI36 chr17: 71,098,359-71,139,134 , GRCh37.p13 chr17: 73,586,764-73,627,539 , GRCh38.p12 chr17: 75,590,683-75,631,459 SMIM5, MYO15B, 1 more genes
    nsv2748809copy number variation2nstd130human NCBI36 chr17: 71,063,780-71,139,134 , GRCh37.p13 chr17: 73,552,185-73,627,539 , GRCh38.p12 chr17: 75,556,104-75,631,459 SMIM5, LLGL2, 2 more genes
    nsv2750885copy number variation1nstd130human NCBI36 chr17: 71,098,863-71,153,309 , GRCh37.p13 chr17: 73,587,268-73,641,714 , GRCh38.p12 chr17: 75,591,187-75,645,634 SMIM5, MYO15B, 2 more genes
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