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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4674131copy number variation1nstd102humanPathogenic GRCh37 chrX: 73,917,544-73,988,312 , GRCh38.p12 chrX: 74,697,709-74,768,477 NEXMIF
    nsv3319002copy number variation1nstd45humanPathogenic GRCh37 chrX: 73,952,691-74,145,287 , GRCh38.p12 chrX: 74,732,856-74,925,452 NEXMIF
    nsv4683741copy number variation2nstd102humanPathogenic, Likely pathogenic GRCh37 chrX: 73,959,220-73,965,505 , GRCh38.p12 chrX: 74,739,385-74,745,670 NEXMIF
    nsv3871572copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 74,016,853-74,178,303 , GRCh38.p12 chrX: 74,797,018-74,958,468 NEXMIF
    nsv3922117copy number variation1nstd102humanUncertain significance NCBI36 chrX: 73,821,830-73,931,566 , GRCh37.p13 chrX: 73,905,105-74,014,841 , GRCh38.p12 chrX: 74,685,270-74,795,006 NEXMIF
    nsv7098727copy number variation1nstd102humanUncertain significance GRCh37 chrX: 73,963,409-73,963,410 , GRCh38 chrX: 74,743,574-74,743,575 NEXMIF
    nsv7092537copy number variation1nstd229human GRCh38 chrX: 74,770,767-74,812,863 , GRCh37.p13 chrX: 73,990,602-74,032,698 NEXMIF
    nsv7092538copy number variation1nstd229human GRCh38 chrX: 74,787,147-74,796,560 , GRCh37.p13 chrX: 74,006,982-74,016,395 NEXMIF
    nsv5416227copy number variation1nstd206human GRCh38 chrX: 74,796,292-74,797,164 , GRCh37.p13 chrX: 74,016,127-74,016,999 NEXMIF
    nsv5423665copy number variation1nstd206human GRCh38 chrX: 74,853,087-74,853,531 , GRCh37.p13 chrX: 74,072,922-74,073,366 NEXMIF
    nsv6111807copy number variation1nstd212human GRCh38 chrX: 74,744,891-74,744,958 , GRCh37.p13 chrX: 73,964,726-73,964,793 NEXMIF
    nsv4765496copy number variation1nstd199human GRCh37 chrX: 73,964,721-73,964,781 , GRCh38.p12 chrX: 74,744,886-74,744,946 NEXMIF
    nsv5879856copy number variation1nstd209human GRCh38 chrX: 74,756,025-74,756,112 , GRCh37.p13 chrX: 73,975,860-73,975,947 NEXMIF
    nsv4771496copy number variation1nstd200human GRCh37 chrX: 73,987,400-73,987,486 , GRCh38.p12 chrX: 74,767,565-74,767,651 NEXMIF
    nsv4032853copy number variation1nstd166human GRCh37.p13 chrX: 73,903,800-74,200,200 , GRCh38.p12 chrX: 74,683,965-74,980,365 NEXMIF
    nsv4038087copy number variation1nstd166human GRCh37.p13 chrX: 74,009,373-74,022,052 , GRCh38.p12 chrX: 74,789,538-74,802,217 NEXMIF
    nsv4517630copy number variation1nstd166human GRCh37.p13 chrX: 74,123,211-74,123,618 , GRCh38.p12 chrX: 74,903,376-74,903,783 NEXMIF
    nsv4046386copy number variation1nstd166human GRCh37.p13 chrX: 73,996,952-73,997,043 , GRCh38.p12 chrX: 74,777,117-74,777,208 NEXMIF
    nsv4374089copy number variation1nstd173human GRCh37 chrX: 73,978,122-74,092,737 , GRCh38.p12 chrX: 74,758,287-74,872,902 NEXMIF
    nsv3201410copy number variation1nstd152human GRCh38 chrX: 74,900,244-74,942,201 , GRCh37.p13 chrX: 74,120,079-74,162,036 NEXMIF
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