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Items: 1 to 20 of 3156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3875090copy number variation1nstd102humanBenign GRCh37 chr4: 165,037,540-165,040,824 , GRCh38.p12 chr4: 164,116,388-164,119,672 MARCHF1
    nsv3873814copy number variation1nstd102humanBenign GRCh37 chr4: 165,203,351-165,206,072 , GRCh38.p12 chr4: 164,282,199-164,284,920 MARCHF1
    nsv3918415copy number variation1nstd102humanLikely benign NCBI36 chr4: 165,447,032-165,683,386 , GRCh38 chr4: 164,306,430-164,542,784 , GRCh37 chr4: 165,227,582-165,463,936 MARCHF1
    nsv4674151copy number variation1nstd102humanUncertain significance GRCh37 chr4: 164,755,286-164,822,323 , GRCh38.p12 chr4: 163,834,134-163,901,171 MARCHF1
    esv4008499copy number variation1estd231human GRCh37 chr4: 165,203,039-165,206,215 , GRCh38.p12 chr4: 164,281,887-164,285,063 MARCHF1
    esv4008488copy number variation1estd231human GRCh37 chr4: 164,658,298-164,659,132 , GRCh38.p12 chr4: 163,737,146-163,737,980 MARCHF1
    esv4008477copy number variation1estd231human GRCh37 chr4: 164,501,940-164,502,253 , GRCh38.p12 chr4: 163,580,788-163,581,101 MARCHF1
    nsv6755219copy number variation1nstd229human GRCh38 chr4: 164,048,529-164,123,386 , GRCh37.p13 chr4: 164,969,681-165,044,538 MARCHF1
    nsv6754948copy number variation1nstd229human GRCh38 chr4: 163,765,457-163,823,269 , GRCh37.p13 chr4: 164,686,609-164,744,421 MARCHF1
    nsv6744023copy number variation1nstd229human GRCh38 chr4: 163,938,401-163,988,800 , GRCh37.p13 chr4: 164,859,553-164,909,952 MARCHF1
    nsv6739931copy number variation1nstd229human GRCh38 chr4: 164,098,947-164,143,690 , GRCh37.p13 chr4: 165,020,099-165,064,842 MARCHF1
    nsv6753709copy number variation1nstd229human GRCh38 chr4: 163,863,077-163,906,981 , GRCh37.p13 chr4: 164,784,229-164,828,133 MARCHF1
    nsv6750990copy number variation1nstd229human GRCh38 chr4: 164,085,292-164,127,317 , GRCh37.p13 chr4: 165,006,444-165,048,469 MARCHF1
    nsv6751459copy number variation1nstd229human GRCh38 chr4: 164,208,601-164,249,100 , GRCh37.p13 chr4: 165,129,753-165,170,252 MARCHF1
    nsv6748508copy number variation1nstd229human GRCh38 chr4: 163,952,851-163,989,501 , GRCh37.p13 chr4: 164,874,003-164,910,653 MARCHF1
    nsv6741548copy number variation1nstd229human GRCh38 chr4: 163,749,793-163,777,044 , GRCh37.p13 chr4: 164,670,945-164,698,196 MARCHF1
    nsv6741868copy number variation1nstd229human GRCh38 chr4: 163,887,817-163,914,845 , GRCh37.p13 chr4: 164,808,969-164,835,997 MARCHF1
    nsv6740651copy number variation1nstd229human GRCh38 chr4: 164,010,175-164,037,151 , GRCh37.p13 chr4: 164,931,327-164,958,303 MARCHF1
    nsv6756273copy number variation1nstd229human GRCh38 chr4: 163,780,332-163,807,034 , GRCh37.p13 chr4: 164,701,484-164,728,186 MARCHF1
    nsv6748189copy number variation1nstd229human GRCh38 chr4: 163,891,659-163,915,745 , GRCh37.p13 chr4: 164,812,811-164,836,897 MARCHF1
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