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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv6979306copy number variation1nstd229human GRCh38 chr17: 63,863,152-63,886,672 , GRCh37.p13 chr17: 61,940,512-61,964,032 CSH2, GH2, 1 more genes
    nsv6637179copy number variation1nstd102humanUncertain significance GRCh37 chr17: 61,838,634-62,465,444 , GRCh38.p12 chr17: 63,761,274-64,469,327 GH2, DDX42, 24 more genes
    nsv6634946copy number variation1nstd227human GRCh37 chr17: 61,954,471-61,983,601 , GRCh38.p12 chr17: 63,877,111-63,906,241 CSH1, GH2
    nsv6624501copy number variation1nstd224human GRCh37 chr17: 61,955,076-61,978,548 , GRCh38.p12 chr17: 63,877,716-63,901,188 CSH1, GH2
    nsv6624500copy number variation8nstd224human GRCh37 chr17: 61,955,076-61,977,248 , GRCh38.p12 chr17: 63,877,716-63,899,888 CSH1, GH2
    nsv6624333copy number variation1nstd224human GRCh37 chr17: 61,947,107-61,978,548 , GRCh38.p12 chr17: 63,869,747-63,901,188 CSH1, CSH2, 1 more genes
    nsv6624104copy number variation16nstd224human GRCh37 chr17: 61,949,917-61,977,248 , GRCh38.p12 chr17: 63,872,557-63,899,888 CSH1, GH2, 1 more genes
    nsv6624098copy number variation1nstd224human GRCh37 chr17: 61,912,893-61,977,248 , GRCh38.p12 chr17: 63,835,533-63,899,888 CSH2, SMARCD2, 3 more genes
    nsv6531564copy number variation1nstd223human GRCh38 chr17: 63,871,301-63,885,900 , GRCh37.p13 chr17: 61,948,661-61,963,260 GH2, CSH2
    nsv6530743copy number variation1nstd223human GRCh38 chr17: 63,873,101-63,881,300 , GRCh37.p13 chr17: 61,950,461-61,958,660 GH2, CSH2
    nsv6529235copy number variation1nstd223human GRCh38 chr17: 63,875,601-63,883,900 , GRCh37.p13 chr17: 61,952,961-61,961,260 GH2
    nsv6529147copy number variation1nstd223human GRCh38 chr17: 63,878,901-63,885,700 , GRCh37.p13 chr17: 61,956,261-61,963,060 GH2
    nsv6528287copy number variation1nstd223human GRCh38 chr17: 63,875,698-63,898,250 , GRCh37.p13 chr17: 61,953,058-61,975,610 GH2, CSH1
    nsv6528262copy number variation1nstd223human GRCh38 chr17: 63,872,701-63,885,900 , GRCh37.p13 chr17: 61,950,061-61,963,260 GH2, CSH2
    nsv6526795copy number variation1nstd223human GRCh38 chr17: 63,863,444-63,901,765 , GRCh37.p13 chr17: 61,940,804-61,979,125 TCAM1P, CSH1, 2 more genes
    nsv6524631copy number variation1nstd223human GRCh38 chr17: 63,870,001-63,907,700 , GRCh37.p13 chr17: 61,947,361-61,985,060 CSH2, CSHL1, 2 more genes
    nsv6524157copy number variation1nstd223human GRCh38 chr17: 63,872,301-63,895,200 , GRCh37.p13 chr17: 61,949,661-61,972,560 CSH1, CSH2, 1 more genes
    nsv6521272copy number variation1nstd223human GRCh38 chr17: 63,869,801-63,907,600 , GRCh37.p13 chr17: 61,947,161-61,984,960 GH2, CSH1, 1 more genes
    nsv6519175copy number variation1nstd223human GRCh38 chr17: 63,866,369-63,889,280 , GRCh37.p13 chr17: 61,943,729-61,966,640 CSH2, GH2
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