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Items: 1 to 20 of 284

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv6677847copy number variation1nstd229human GRCh38 chr1: 225,839,847-225,854,021 , GRCh37.p13 chr1: 226,027,548-226,041,722 EPHX1, TMEM63A
    nsv6672360copy number variation1nstd229human GRCh38 chr1: 225,848,590-225,865,592 , GRCh37.p13 chr1: 226,036,291-226,053,292 TMEM63A
    nsv6669177copy number variation1nstd229human GRCh38 chr1: 225,856,735-225,861,500 , GRCh37.p13 chr1: 226,044,436-226,049,200 TMEM63A
    nsv6665951copy number variation1nstd229human GRCh38 chr1: 225,864,516-225,866,805 , GRCh37.p13 chr1: 226,052,216-226,054,505 TMEM63A
    nsv6663001copy number variation1nstd229human GRCh38 chr1: 225,871,737-225,871,896 , GRCh37.p13 chr1: 226,059,437-226,059,596 TMEM63A
    nsv6661018copy number variation1nstd229human GRCh38 chr1: 225,859,512-225,864,038 , GRCh37.p13 chr1: 226,047,212-226,051,738 TMEM63A
    nsv6658310copy number variation1nstd229human GRCh38 chr1: 225,856,501-225,864,300 , GRCh37.p13 chr1: 226,044,202-226,052,000 TMEM63A
    nsv6658215copy number variation1nstd229human GRCh38 chr1: 225,804,601-225,930,400 , GRCh37.p13 chr1: 225,992,303-226,118,100 LEFTY1, EPHX1, 3 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6325680copy number variation1nstd223human GRCh38 chr1: 225,830,730-225,858,590 , GRCh37.p13 chr1: 226,018,431-226,046,290 TMEM63A, EPHX1
    nsv6325441copy number variation1nstd223human GRCh38 chr1: 225,868,540-225,870,298 , GRCh37.p13 chr1: 226,056,240-226,057,998 TMEM63A
    nsv6325378copy number variation1nstd223human GRCh38 chr1: 225,859,511-225,864,037 , GRCh37.p13 chr1: 226,047,211-226,051,737 TMEM63A
    nsv6324615copy number variation1nstd223human GRCh38 chr1: 221,964,560-227,275,239 , GRCh37.p13 chr1: 222,137,902-227,462,940 LEFTY2, HHIPL2, 109 more genes
    nsv6322799copy number variation1nstd223human GRCh38 chr1: 225,841,308-225,841,833 , GRCh37.p13 chr1: 226,029,009-226,029,534 EPHX1, TMEM63A
    nsv6313779copy number variation1nstd102humanPathogenic GRCh37 chr1: 221,303,919-227,461,343 , GRCh38.p12 chr1: 221,130,577-227,273,642 ENAH, HHIPL2, 119 more genes
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