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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137837copy number variation1nstd102humanPathogenic GRCh37 chrX: 10,491,132-10,535,643 , GRCh38.p12 chrX: 10,523,092-10,567,603 MID1
    nsv7098482copy number variation1nstd102humanPathogenic GRCh37 chrX: 10,491,112-10,535,587 , GRCh38.p12 chrX: 10,523,072-10,567,547 MID1
    nsv7098207copy number variation1nstd102humanPathogenic GRCh37 chrX: 10,417,408-10,423,137 , GRCh38.p12 chrX: 10,449,368-10,455,097 MID1
    nsv3904398copy number variation1nstd102humanPathogenic NCBI36 chrX: 10,687,116-10,993,611 , GRCh37 chrX: 10,727,116-11,083,690 , GRCh38 chrX: 10,759,076-11,065,570 MID1
    nsv3872913copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 10,381,839-10,487,986 , GRCh38.p12 chrX: 10,413,799-10,519,946 MID1
    nsv7098208copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chrX: 10,450,500-10,450,688 , GRCh38.p12 chrX: 10,482,460-10,482,648 MID1
    nsv3879567copy number variation1nstd102humanBenign GRCh37 chrX: 10,525,394-10,530,851 , GRCh38.p12 chrX: 10,557,354-10,562,811 MID1
    nsv3872828copy number variation1nstd102humanBenign GRCh37 chrX: 10,530,487-10,535,838 , GRCh38.p12 chrX: 10,562,447-10,567,798 MID1
    nsv3883114copy number variation1nstd102humanBenign GRCh37 chrX: 10,530,487-10,530,851 , GRCh38.p12 chrX: 10,562,447-10,562,811 MID1
    nsv3874394copy number variation1nstd102humanLikely benign GRCh37 chrX: 10,842,514-10,978,163 , GRCh38.p12 chrX: 10,824,395-10,960,043 MID1
    nsv3874607copy number variation1nstd102humanLikely benign GRCh37 chrX: 10,851,227-10,978,163 , GRCh38.p12 chrX: 10,833,108-10,960,043 MID1
    nsv3890821copy number variation2nstd102humanUncertain significance, Likely benign NCBI36 chrX: 10,361,388-10,430,366 , GRCh37 chrX: 10,401,388-10,470,366 , GRCh38 chrX: 10,433,348-10,502,326 MID1
    nsv3874271copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,818,107-11,070,209 , GRCh38.p12 chrX: 10,799,988-11,052,089 MID1
    nsv6636062copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,622,750-10,816,469 , GRCh38.p12 chrX: 10,654,710-10,798,350 MID1
    nsv4674078copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,462,005-10,485,205 , GRCh38.p12 chrX: 10,493,965-10,517,165 MID1
    nsv4674508copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,628,212-11,011,701 , GRCh38.p12 chrX: 10,660,172-10,993,581 MID1
    nsv3881201copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,830,655-11,053,979 , GRCh38.p12 chrX: 10,812,536-11,035,859 MID1
    nsv6290432copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,843,953-11,025,900 , GRCh38.p12 chrX: 10,825,834-11,007,780 MID1
    nsv3881121copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,843,658-11,016,962 , GRCh38.p12 chrX: 10,825,539-10,998,842 MID1
    nsv4728393copy number variation1nstd102humanUncertain significance GRCh37 chrX: 10,843,952-11,016,962 , GRCh38.p12 chrX: 10,825,833-10,998,842 MID1
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