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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6131176insertion1nstd186human GRCh37 chr19: 19,321,811-19,321,811 , GRCh38.p12 chr19: 19,211,002-19,211,002 NCAN
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5937070copy number variation1nstd209human GRCh38 chr19: 19,249,108-19,249,399 , GRCh37.p13 chr19: 19,359,917-19,360,208 NCAN
    nsv5885352copy number variation1nstd209human GRCh38 chr19: 19,235,399-19,237,798 , GRCh37.p13 chr19: 19,346,208-19,348,607 NCAN
    nsv5730486mobile element insertion1nstd211human GRCh38 chr19: 19,247,016-19,247,016 , GRCh37.p13 chr19: 19,357,825-19,357,825 NCAN
    nsv5653702insertion1nstd207human GRCh38 chr19: 19,211,002-19,211,002 , GRCh37.p13 chr19: 19,321,811-19,321,811 NCAN
    nsv5563048mobile element insertion1nstd206human GRCh38 chr19: 19,247,016-19,247,067 , GRCh37.p13 chr19: 19,357,825-19,357,876 NCAN
    nsv5542682insertion1nstd206human GRCh38 chr19: 19,211,002-19,211,002 , GRCh37.p13 chr19: 19,321,811-19,321,811 NCAN
    nsv5518268copy number variation1nstd206human GRCh38 chr19: 19,243,430-19,243,940 , GRCh37.p13 chr19: 19,354,239-19,354,749 NCAN
    nsv5321204copy number variation1nstd204human GRCh38.p13 chr19: 19,243,332-19,243,805 , GRCh37.p13 chr19: 19,354,141-19,354,614 NCAN
    nsv5299782copy number variation1nstd204human GRCh38.p13 chr19: 18,706,301-19,688,800 , GRCh37.p13 chr19: 18,817,111-19,799,609 , HOMER3-AS1, 37 more genes
    nsv5167252mobile element insertion1nstd203human GRCh38 chr19: 19,210,190-19,210,209 , GRCh37.p13 chr19: 19,320,999-19,321,018 NCAN
    nsv5166704mobile element insertion1nstd203human GRCh38 chr19: 19,211,002-19,211,036 , GRCh37.p13 chr19: 19,321,811-19,321,845 NCAN
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019459copy number variation1nstd200human GRCh38 chr19: 19,252,285-19,256,535 , GRCh37.p13 chr19: 19,363,094-19,367,344 HAPLN4, NCAN
    nsv5019458copy number variation1nstd200human GRCh38 chr19: 19,247,335-19,253,188 , GRCh37.p13 chr19: 19,358,144-19,363,997 NCAN, HAPLN4
    nsv5019457copy number variation1nstd200human GRCh38 chr19: 19,242,534-19,243,827 , GRCh37.p13 chr19: 19,353,343-19,354,636 NCAN
    nsv5014663copy number variation1nstd200human GRCh38 chr19: 19,230,197-19,230,584 , GRCh37.p13 chr19: 19,341,006-19,341,393 NCAN
    nsv5014660copy number variation1nstd200human GRCh38 chr19: 19,105,820-19,389,022 , GRCh37.p13 chr19: 19,216,629-19,499,831 TMEM161A, HAPLN4, 12 more genes
    nsv4760786insertion1nstd199human GRCh37 chr19: 19,321,821-19,321,821 , GRCh38.p12 chr19: 19,211,012-19,211,012 NCAN
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