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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058430inversion1nstd229human GRCh38 chr12: 74,653,520-74,824,146 , GRCh37.p13 chr12: 75,047,300-75,217,926 LOC387869, LOC100128673
    nsv6936763copy number variation1nstd229human GRCh38 chr12: 74,702,542-74,814,930 , GRCh37.p13 chr12: 75,096,322-75,208,710 LOC100128673
    nsv6593094inversion1nstd223human GRCh38 chr12: 66,057,683-74,924,429 , GRCh37.p13 chr12: 66,451,463-75,318,209 MYRFL, OSBPL9P5, 119 more genes
    nsv6592639inversion1nstd223human GRCh38 chr12: 66,057,685-75,569,831 , GRCh37.p13 chr12: 66,451,465-75,963,611 RPL39P28, LOC105369842, 131 more genes
    nsv6587098inversion1nstd223human GRCh38 chr12: 70,939,082-79,478,721 , GRCh37.p13 chr12: 71,332,862-79,872,501 , H3P35, 83 more genes
    nsv6584449inversion1nstd223human GRCh38 chr12: 66,057,683-75,201,071 , GRCh37.p13 chr12: 66,451,463-75,594,851 LOC101928002, LOC100422438, 121 more genes
    nsv6582770inversion1nstd223human GRCh38 chr12: 66,057,683-75,778,623 , GRCh37.p13 chr12: 66,451,463-76,172,403 CPSF6, TBC1D15, 135 more genes
    nsv6579681inversion1nstd223human GRCh38 chr12: 66,057,593-76,009,153 , GRCh37.p13 chr12: 66,451,373-76,402,933 SNORA113, LOC100509370, 138 more genes
    nsv6578333inversion1nstd223human GRCh38 chr12: 66,057,684-75,311,659 , GRCh37.p13 chr12: 66,451,464-75,705,439 SNORA70G, LOC105369823, 126 more genes
    nsv6577012inversion1nstd223human GRCh38 chr12: 66,057,684-75,476,019 , GRCh37.p13 chr12: 66,451,464-75,869,799 LOC105369839, SLC35E3, 128 more genes
    nsv6576583inversion1nstd223human GRCh38 chr12: 66,057,593-75,139,035 , GRCh37.p13 chr12: 66,451,373-75,532,815 SZRD1P1, KCNC2, 121 more genes
    nsv6575795inversion1nstd223human GRCh38 chr12: 66,057,683-75,220,512 , GRCh37.p13 chr12: 66,451,463-75,614,292 TRHDE, IL26, 121 more genes
    nsv6459218copy number variation1nstd223human GRCh38 chr12: 74,724,859-74,737,120 , GRCh37.p13 chr12: 75,118,639-75,130,900 LOC100128673
    nsv6314203copy number variation1nstd102humanUncertain significance GRCh37 chr12: 75,068,633-75,504,887 , GRCh38.p12 chr12: 74,674,853-75,111,107 LOC105369842, LOC100128673, 2 more genes
    nsv6291127copy number variation1nstd102humanPathogenic GRCh37 chr12: 70,084,476-77,065,764 , GRCh38.p12 chr12: 69,690,696-76,671,984 LOC100130268, RNU6-1012P, 78 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132712copy number variation1nstd213human GRCh37 chr12: 74,000,000-75,430,001 , GRCh38.p12 chr12: 73,606,220-75,036,221 ATXN7L3B, LINC02394, 12 more genes
    nsv6132436copy number variation1nstd213human GRCh37 chr12: 74,840,000-75,220,001 , GRCh38.p12 chr12: 74,446,220-74,826,221 LOC387869, ATXN7L3B, 2 more genes
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv6039139copy number variation1nstd212human GRCh38 chr12: 74,728,106-74,728,328 , GRCh37.p13 chr12: 75,121,886-75,122,108 LOC100128673
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