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Items: 1 to 20 of 78

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076079inversion1nstd229human GRCh38 chr16: 9,015,595-14,846,246 , GRCh37.p13 chr16: 9,109,452-14,940,103 LOC105371093, RNU6-633P, 100 more genes
    nsv6965574copy number variation1nstd229human GRCh38 chr16: 14,268,501-14,452,500 , GRCh37.p13 chr16: 14,362,358-14,546,357 PARN, MIR193B, 4 more genes
    nsv6961268copy number variation1nstd229human GRCh38 chr16: 14,274,401-14,452,100 , GRCh37.p13 chr16: 14,368,258-14,545,957 TRT-CGT2-1, MIR193BHG, 4 more genes
    nsv6637442copy number variation1nstd102humanLikely pathogenic GRCh37 chr16: 14,365,745-17,052,798 , GRCh38.p12 chr16: 14,271,888-16,958,941 ABCC6, ABCC1, 69 more genes
    nsv6637429copy number variation1nstd102humanPathogenic GRCh37 chr16: 4,380,767-30,445,350 , GRCh38.p12 chr16: 4,330,766-30,434,029 MIR6511B2, ACSM5, 535 more genes
    nsv6501877copy number variation1nstd223human GRCh38 chr16: 14,286,497-14,309,905 , GRCh37.p13 chr16: 14,380,354-14,403,762 MIR193BHG, MIR365A, 1 more genes
    nsv6309988copy number variation1nstd102humanUncertain significance GRCh37 chr16: 13,915,808-14,724,045 , GRCh38.p12 chr16: 13,821,951-14,630,188 TRT-CGT2-1, RN7SL274P, 14 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6133257copy number variation1nstd213human GRCh37 chr16: 14,270,000-14,900,001 , GRCh38.p12 chr16: 14,176,143-14,806,144 , GRCh38.p12 chr16|NT_187607.1: 1-565,201 , PARN, 25 more genes
    nsv6133178copy number variation1nstd213human GRCh37 chr16: 13,470,000-14,990,001 , GRCh38.p12 chr16: 13,376,143-14,896,144 , ERCC4, 26 more genes
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5657552insertion1nstd207human GRCh38 chr16: 14,302,681-14,302,681 , GRCh37.p13 chr16: 14,396,538-14,396,538 MIR193B, MIR193BHG
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4668157copy number variation1nstd186human GRCh37 chr16: 14,394,601-14,397,500 , GRCh38.p12 chr16: 14,300,744-14,303,643 MIR193B, MIR193BHG
    nsv4619528copy number variation1nstd183human GRCh37 chr16: 14,394,601-14,397,500 , GRCh38.p12 chr16: 14,300,744-14,303,643 MIR193BHG, MIR193B
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv3918732copy number variation1nstd102humanPathogenic GRCh37 chr16: 12,061,688-15,256,745 , GRCh38 chr16: 11,967,831-15,162,888 , NCBI36 chr16: 11,969,189-15,164,246 LOC105371087, BFAR, 62 more genes
    nsv3918288copy number variation1nstd102humanLikely benign GRCh38 chr16: 14,140,498-14,686,337 , NCBI36 chr16: 14,141,856-14,687,695 , GRCh37 chr16: 14,234,355-14,780,194 BFAR, TVP23CP2, 12 more genes
    nsv3917207copy number variation1nstd102humanLikely pathogenic NCBI36 chr16: 11,953,825-15,187,557 , GRCh37 chr16: 12,046,324-15,280,056 , GRCh38 chr16: 11,952,467-15,186,199 TNFRSF17, ERCC4, 63 more genes
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