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Items: 1 to 20 of 386

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7050559inversion1nstd229human GRCh38 chr6: 137,097,512-142,245,470 , GRCh37.p13 chr6: 137,418,649-142,566,607 LINC03004, LOC107986651, 64 more genes
    nsv7048636inversion1nstd229human GRCh38 chr6: 138,740,942-138,941,272 , GRCh37.p13 chr6: 139,062,079-139,262,409 CCDC28A, LOC107986650, 4 more genes
    nsv6816363copy number variation1nstd229human GRCh38 chr6: 138,869,688-138,870,437 , GRCh37.p13 chr6: 139,190,825-139,191,574 ECT2L
    nsv6815795copy number variation1nstd229human GRCh38 chr6: 138,837,077-138,839,368 , GRCh37.p13 chr6: 139,158,214-139,160,505 ECT2L
    nsv6815597copy number variation1nstd229human GRCh38 chr6: 138,788,653-138,800,406 , GRCh37.p13 chr6: 139,109,790-139,121,543 CCDC28A, ECT2L
    nsv6811912copy number variation1nstd229human GRCh38 chr6: 137,801,388-140,356,633 , GRCh37.p13 chr6: 138,122,525-140,677,770 TXLNB, LOC100129844, 38 more genes
    nsv6811869copy number variation1nstd229human GRCh38 chr6: 138,787,393-138,798,739 , GRCh37.p13 chr6: 139,108,530-139,119,876 CCDC28A, ECT2L
    nsv6811108copy number variation1nstd229human GRCh38 chr6: 138,878,594-138,878,711 , GRCh37.p13 chr6: 139,199,731-139,199,848 ECT2L
    nsv6805044copy number variation1nstd229human GRCh38 chr6: 138,806,748-138,807,114 , GRCh37.p13 chr6: 139,127,885-139,128,251 ECT2L
    nsv6803431copy number variation1nstd229human GRCh38 chr6: 138,710,644-138,866,827 , GRCh37.p13 chr6: 139,031,781-139,187,964 ACKR4P1, CCDC28A-AS1, 2 more genes
    nsv6802838copy number variation1nstd229human GRCh38 chr6: 138,834,019-138,840,975 , GRCh37.p13 chr6: 139,155,156-139,162,112 ECT2L
    nsv6802508copy number variation1nstd229human GRCh38 chr6: 138,864,885-138,868,754 , GRCh37.p13 chr6: 139,186,022-139,189,891 ECT2L
    nsv6801251copy number variation1nstd229human GRCh38 chr6: 138,795,564-138,795,672 , GRCh37.p13 chr6: 139,116,701-139,116,809 ECT2L
    nsv6799931copy number variation1nstd229human GRCh38 chr6: 138,798,471-138,802,667 , GRCh37.p13 chr6: 139,119,608-139,123,804 ECT2L
    nsv6799361copy number variation1nstd229human GRCh38 chr6: 138,825,212-138,835,179 , GRCh37.p13 chr6: 139,146,349-139,156,316 ECT2L
    nsv6798967copy number variation1nstd229human GRCh38 chr6: 138,858,290-138,861,139 , GRCh37.p13 chr6: 139,179,427-139,182,276 ECT2L
    nsv6636436copy number variation1nstd102humanUncertain significance GRCh37 chr6: 139,063,032-139,273,184 , GRCh38.p12 chr6: 138,741,895-138,952,047 ECT2L, LOC107986650, 4 more genes
    nsv6619537copy number variation1nstd223human GRCh38 chr6: 138,885,201-138,886,600 , GRCh37.p13 chr6: 139,206,338-139,207,737 ECT2L
    nsv6618300copy number variation1nstd223human GRCh38 chr6: 138,875,885-138,884,365 , GRCh37.p13 chr6: 139,197,022-139,205,502 ECT2L
    nsv6615445copy number variation1nstd223human GRCh38 chr6: 138,883,585-138,902,621 , GRCh37.p13 chr6: 139,204,722-139,223,758 ECT2L, REPS1, 1 more genes
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