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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5519407copy number variation1nstd206human GRCh38 chr15: 78,864,020-78,864,591 , GRCh37.p13 chr15: 79,156,362-79,156,933 RPL21P116
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5001887copy number variation1nstd200human GRCh38 chr15: 78,864,020-78,864,591 , GRCh37.p13 chr15: 79,156,362-79,156,933 RPL21P116
    nsv5001886copy number variation1nstd200human GRCh38 chr15: 78,861,483-78,861,573 , GRCh37.p13 chr15: 79,153,825-79,153,915 RPL21P116
    nsv4992298copy number variation1nstd200human GRCh38 chr15: 73,152,590-82,101,178 , GRCh37.p13 chr15: 73,444,931-82,393,519 , SNUPN, 215 more genes
    nsv4856000copy number variation1nstd200human GRCh37 chr15: 79,156,362-79,156,933 , GRCh38.p12 chr15: 78,864,020-78,864,591 RPL21P116
    nsv4531953copy number variation1nstd166human GRCh37.p13 chr15: 79,156,362-79,156,933 , GRCh38.p12 chr15: 78,864,020-78,864,591 RPL21P116
    nsv4240333copy number variation1nstd166human GRCh37.p13 chr15: 79,148,000-79,159,000 , GRCh38.p12 chr15: 78,855,658-78,866,658 TRK-CTT1-2, RPL21P116
    nsv4238597copy number variation1nstd166human GRCh37.p13 chr15: 79,153,825-79,153,915 , GRCh38.p12 chr15: 78,861,483-78,861,573 RPL21P116
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918992copy number variation1nstd102humanPathogenic NCBI36 chr15: 75,141,730-95,931,047 , GRCh37.p13 chr15: 77,354,675-98,130,043 , GRCh38.p12 chr15: 77,062,333-97,586,813 TLNRD1, FES, 403 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3918013copy number variation1nstd102humanLikely benign NCBI36 chr15: 76,278,105-76,992,310 , GRCh38 chr15: 78,198,708-78,912,913 , GRCh37 chr15: 78,491,050-79,205,255 PSMA4, LOC646934, 24 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 GAPDHP61, SNORD18B, 840 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915210copy number variation1nstd102humanUncertain significance NCBI36 chr15: 28,207,117-100,338,915 , GRCh37.p13 chr15: 30,419,825-102,521,392 , GRCh38.p12 chr15: 30,127,622-101,981,189 RPL21P113, LOC112268152, 1428 more genes
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