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Items: 1 to 20 of 252

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6644468copy number variation1nstd229human GRCh38 chr1: 169,371,980-169,409,874 , GRCh37.p13 chr1: 169,341,218-169,379,112 CCDC181, BLZF1
    nsv6644465copy number variation1nstd229human GRCh38 chr1: 169,282,980-169,437,910 , GRCh37.p13 chr1: 169,252,218-169,407,148 CCDC181, BLZF1, 1 more genes
    nsv6644464copy number variation1nstd229human GRCh38 chr1: 169,278,706-169,386,194 , GRCh37.p13 chr1: 169,247,944-169,355,432 BLZF1, NME7
    nsv6644401copy number variation1nstd229human GRCh38 chr1: 169,394,901-169,399,100 , GRCh37.p13 chr1: 169,364,139-169,368,338 CCDC181, BLZF1
    nsv6644297copy number variation1nstd229human GRCh38 chr1: 169,337,783-169,372,210 , GRCh37.p13 chr1: 169,307,021-169,341,448 BLZF1, NME7
    nsv6644256copy number variation1nstd229human GRCh38 chr1: 168,110,598-170,953,728 , GRCh37.p13 chr1: 168,079,836-170,922,869 SELL, RPL7AP21, 55 more genes
    nsv6637036copy number variation1nstd102humanUncertain significance GRCh37 chr1: 168,675,820-169,363,333 , GRCh38.p12 chr1: 168,706,582-169,394,095 LOC101928596, CCDC181, 10 more genes
    nsv6625915copy number variation1nstd224human GRCh37 chr1: 169,256,570-169,377,123 , GRCh38.p12 chr1: 169,287,332-169,407,885 BLZF1, NME7, 1 more genes
    nsv6625874copy number variation1nstd224human GRCh37 chr1: 169,204,377-169,346,173 , GRCh38.p12 chr1: 169,235,139-169,376,935 BLZF1, NME7
    nsv6536449inversion1nstd223human GRCh38 chr1: 169,227,760-169,402,827 , GRCh37.p13 chr1: 169,196,998-169,372,065 BLZF1, NME7, 1 more genes
    nsv6331125copy number variation1nstd223human GRCh38 chr1: 169,371,873-169,372,264 , GRCh37.p13 chr1: 169,341,111-169,341,502 BLZF1
    nsv6329457copy number variation1nstd223human GRCh38 chr1: 169,377,501-169,378,400 , GRCh37.p13 chr1: 169,346,739-169,347,638 BLZF1
    nsv6328305copy number variation1nstd223human GRCh38 chr1: 169,373,451-169,374,389 , GRCh37.p13 chr1: 169,342,689-169,343,627 BLZF1
    nsv6327715copy number variation1nstd223human GRCh38 chr1: 169,381,001-169,382,000 , GRCh37.p13 chr1: 169,350,239-169,351,238 BLZF1
    nsv6320440copy number variation1nstd223human GRCh38 chr1: 169,379,301-169,380,300 , GRCh37.p13 chr1: 169,348,539-169,349,538 BLZF1
    nsv6313719copy number variation1nstd102humanPathogenic GRCh37 chr1: 162,330,810-171,532,331 , GRCh38.p12 chr1: 162,361,020-171,563,192 LOC100420658, LOC105371610, 167 more genes
    nsv6313602copy number variation1nstd102humanPathogenic GRCh37 chr1: 167,391,422-171,843,613 , GRCh38.p12 chr1: 167,422,185-171,874,473 DCAF6, SELE, 101 more genes
    nsv6296526copy number variation1nstd186human GRCh37 chr1: 169,361,070-169,361,134 , GRCh38.p12 chr1: 169,391,832-169,391,896 BLZF1
    nsv6139479copy number variation1nstd206human GRCh38 chr1: 169,391,832-169,391,896 , GRCh37.p13 chr1: 169,361,070-169,361,134 BLZF1
    nsv6133937copy number variation1nstd213human GRCh37 chr1: 167,800,000-169,660,001 , GRCh38.p12 chr1: 167,830,762-169,690,860 XCL2, TBX19, 38 more genes
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