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Items: 1 to 20 of 164

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097208copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,736,648-53,845,433 , GRCh38.p12 chr3: 53,702,621-53,811,406 CHDH, CACNA1D
    nsv7097207copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,529,194-53,845,433 , GRCh38.p12 chr3: 53,495,167-53,811,406 CHDH, CACNA1D
    nsv7096962copy number variation1nstd102humanUncertain significance GRCh37 chr3: 53,820,829-53,845,433 , GRCh38.p12 chr3: 53,786,802-53,811,406 CACNA1D, CHDH
    nsv7096813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 52,018,081-53,845,433 , GRCh38.p12 chr3: 51,984,065-53,811,406 DNAH1, BAP1, 62 more genes
    nsv6716707copy number variation1nstd229human GRCh38 chr3: 53,767,647-53,833,678 , GRCh37.p13 chr3: 53,801,674-53,867,705 CACNA1D, CHDH
    nsv6712270copy number variation1nstd229human GRCh38 chr3: 53,689,493-54,361,248 , GRCh37.p13 chr3: 53,723,520-54,395,275 CACNA1D, SELENOK, 6 more genes
    nsv6709974copy number variation1nstd229human GRCh38 chr3: 53,819,551-53,823,643 , GRCh37.p13 chr3: 53,853,578-53,857,670 CHDH
    nsv6708718copy number variation1nstd229human GRCh38 chr3: 53,828,846-53,852,221 , GRCh37.p13 chr3: 53,862,873-53,886,248 CHDH, IL17RB
    nsv6707357copy number variation1nstd229human GRCh38 chr3: 53,818,721-53,822,984 , GRCh37.p13 chr3: 53,852,748-53,857,011 CHDH
    nsv6699023copy number variation1nstd229human GRCh38 chr3: 52,811,798-54,282,378 , GRCh37.p13 chr3: 52,845,814-54,316,405 LOC105377095, SERBP1P3, 22 more genes
    nsv6375190copy number variation1nstd223human GRCh38 chr3: 53,823,983-53,901,628 , GRCh37.p13 chr3: 53,858,010-53,935,655 IL17RB, SELENOK, 2 more genes
    nsv6369827copy number variation1nstd223human GRCh38 chr3: 52,164,358-54,467,618 , GRCh37.p13 chr3: 52,198,374-54,501,645 SEMA3G, STAB1, 61 more genes
    nsv6135017copy number variation1nstd213human GRCh37 chr3: 53,320,000-54,590,001 , GRCh38.p12 chr3: 53,285,982-54,555,974 CACNA1D, CHDH, 11 more genes
    nsv5993663copy number variation1nstd212human GRCh38 chr3: 53,840,314-53,840,450 , GRCh37.p13 chr3: 53,874,341-53,874,477 CHDH
    nsv5993662copy number variation1nstd212human GRCh38 chr3: 53,817,875-53,818,224 , GRCh37.p13 chr3: 53,851,902-53,852,251 CHDH
    nsv5953705insertion1nstd209human GRCh38 chr3: 53,810,786-53,810,786 , GRCh37.p13 chr3: 53,844,813-53,844,813 CHDH, CACNA1D
    nsv5692573mobile element insertion1nstd211human GRCh38 chr3: 53,820,097-53,820,097 , GRCh37.p13 chr3: 53,854,124-53,854,124 CHDH
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5446187copy number variation1nstd206human GRCh38 chr3: 53,819,556-53,819,607 , GRCh37.p13 chr3: 53,853,583-53,853,634 CHDH
    nsv5400246mobile element insertion1nstd206human GRCh38 chr3: 53,820,097-53,820,148 , GRCh37.p13 chr3: 53,854,124-53,854,175 CHDH
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