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Items: 1 to 20 of 581

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147874insertion1nstd232human GRCh37.p13 chr17: 12,866,995-12,866,995 , GRCh38.p12 chr17: 12,963,678-12,963,678 ARHGAP44
    nsv7077282inversion1nstd229human GRCh38 chr17: 12,800,282-12,803,568 , GRCh37.p13 chr17: 12,703,599-12,706,885 ARHGAP44
    nsv7075649inversion1nstd229human GRCh38 chr17: 12,811,820-12,811,899 , GRCh37.p13 chr17: 12,715,137-12,715,216 ARHGAP44
    nsv6995769copy number variation1nstd229human GRCh38 chr17: 12,884,733-13,059,494 , GRCh37.p13 chr17: 12,788,050-12,962,811 ARHGAP44, MIR1269B, 1 more genes
    nsv6995651copy number variation1nstd229human GRCh38 chr17: 12,931,667-12,937,964 , GRCh37.p13 chr17: 12,834,984-12,841,281 ARHGAP44
    nsv6993604copy number variation1nstd229human GRCh38 chr17: 12,929,505-12,933,094 , GRCh37.p13 chr17: 12,832,822-12,836,411 ARHGAP44
    nsv6993141copy number variation1nstd229human GRCh38 chr17: 12,820,901-12,823,000 , GRCh37.p13 chr17: 12,724,218-12,726,317 ARHGAP44
    nsv6991644copy number variation1nstd229human GRCh38 chr17: 12,834,792-12,846,624 , GRCh37.p13 chr17: 12,738,109-12,749,941 ARHGAP44
    nsv6990629copy number variation1nstd229human GRCh38 chr17: 12,907,864-12,908,047 , GRCh37.p13 chr17: 12,811,181-12,811,364 ARHGAP44
    nsv6988010copy number variation1nstd229human GRCh38 chr17: 12,938,583-13,070,068 , GRCh37.p13 chr17: 12,841,900-12,973,385 ELAC2, ARHGAP44
    nsv6987644copy number variation1nstd229human GRCh38 chr17: 12,786,907-12,836,417 , GRCh37.p13 chr17: 12,690,224-12,739,734 ARHGAP44, ARHGAP44-AS1
    nsv6987508copy number variation1nstd229human GRCh38 chr17: 12,786,677-12,803,608 , GRCh37.p13 chr17: 12,689,994-12,706,925 ARHGAP44, ARHGAP44-AS1
    nsv6986983copy number variation1nstd229human GRCh38 chr17: 12,922,673-12,922,892 , GRCh37.p13 chr17: 12,825,990-12,826,209 ARHGAP44
    nsv6983628copy number variation1nstd229human GRCh38 chr17: 12,799,900-12,833,890 , GRCh37.p13 chr17: 12,703,217-12,737,207 ARHGAP44
    nsv6981797copy number variation1nstd229human GRCh38 chr17: 12,800,443-12,815,794 , GRCh37.p13 chr17: 12,703,760-12,719,111 ARHGAP44
    nsv6979700copy number variation1nstd229human GRCh38 chr17: 12,558,301-12,936,100 , GRCh37.p13 chr17: 12,461,618-12,839,417 ARHGAP44-AS1, MIR1269B, 5 more genes
    nsv6979650copy number variation1nstd229human GRCh38 chr17: 12,922,021-12,923,040 , GRCh37.p13 chr17: 12,825,338-12,826,357 ARHGAP44
    nsv6979639copy number variation1nstd229human GRCh38 chr17: 12,864,392-12,876,494 , GRCh37.p13 chr17: 12,767,709-12,779,811 ARHGAP44
    nsv6979351copy number variation1nstd229human GRCh38 chr17: 12,688,917-15,327,390 , GRCh37.p13 chr17: 12,592,234-15,230,707 PMP22, COX10-DT, 32 more genes
    nsv6978867copy number variation1nstd229human GRCh38 chr17: 12,931,777-12,937,966 , GRCh37.p13 chr17: 12,835,094-12,841,283 ARHGAP44
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