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Items: 1 to 20 of 596

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077230inversion1nstd229human GRCh38 chr9: 70,051,468-70,057,493 , GRCh37.p13 chr9: 72,666,384-72,672,409 MAMDC2
    nsv7076565inversion1nstd229human GRCh38 chr9: 70,059,950-70,059,961 , GRCh37.p13 chr9: 72,674,866-72,674,877 MAMDC2
    nsv7069427inversion1nstd229human GRCh38 chr9: 70,206,155-70,206,236 , GRCh37.p13 chr9: 72,821,071-72,821,152 MAMDC2
    nsv7068980inversion1nstd229human GRCh38 chr9: 70,155,316-70,155,356 , GRCh37.p13 chr9: 72,770,232-72,770,272 MAMDC2, MAMDC2-AS1
    nsv6877163copy number variation1nstd229human GRCh38 chr9: 70,180,801-70,184,300 , GRCh37.p13 chr9: 72,795,717-72,799,216 MAMDC2
    nsv6877056copy number variation1nstd229human GRCh38 chr9: 70,206,301-70,215,600 , GRCh37.p13 chr9: 72,821,217-72,830,516 SMC5-DT, RPL24P8, 1 more genes
    nsv6876898copy number variation1nstd229human GRCh38 chr9: 70,139,801-70,146,400 , GRCh37.p13 chr9: 72,754,717-72,761,316 MAMDC2
    nsv6876182copy number variation1nstd229human GRCh38 chr9: 70,015,508-70,112,451 , GRCh37.p13 chr9: 72,630,424-72,727,367 MAMDC2
    nsv6876073copy number variation1nstd229human GRCh38 chr9: 70,141,843-70,142,031 , GRCh37.p13 chr9: 72,756,759-72,756,947 MAMDC2
    nsv6873470copy number variation1nstd229human GRCh38 chr9: 70,225,601-70,561,100 , GRCh37.p13 chr9: 72,840,517-73,176,016 MAMDC2, KLF9, 5 more genes
    nsv6872084copy number variation1nstd229human GRCh38 chr9: 70,113,851-70,121,301 , GRCh37.p13 chr9: 72,728,767-72,736,217 MAMDC2
    nsv6870793copy number variation1nstd229human GRCh38 chr9: 69,925,801-70,146,600 , GRCh37.p13 chr9: 72,540,717-72,761,516 MAMDC2
    nsv6870043copy number variation1nstd229human GRCh38 chr9: 70,146,929-70,148,985 , GRCh37.p13 chr9: 72,761,845-72,763,901 MAMDC2
    nsv6869687copy number variation1nstd229human GRCh38 chr9: 70,211,676-70,214,057 , GRCh37.p13 chr9: 72,826,592-72,828,973 MAMDC2
    nsv6869596copy number variation1nstd229human GRCh38 chr9: 70,206,601-70,212,600 , GRCh37.p13 chr9: 72,821,517-72,827,516 MAMDC2
    nsv6869035copy number variation1nstd229human GRCh38 chr9: 70,177,493-70,180,279 , GRCh37.p13 chr9: 72,792,409-72,795,195 MAMDC2
    nsv6868854copy number variation1nstd229human GRCh38 chr9: 70,050,201-70,146,300 , GRCh37.p13 chr9: 72,665,117-72,761,216 MAMDC2
    nsv6868213copy number variation1nstd229human GRCh38 chr9: 70,048,917-70,116,376 , GRCh37.p13 chr9: 72,663,833-72,731,292 MAMDC2
    nsv6868158copy number variation1nstd229human GRCh38 chr9: 70,060,201-70,060,369 , GRCh37.p13 chr9: 72,675,117-72,675,285 MAMDC2
    nsv6867896copy number variation1nstd229human GRCh38 chr9: 70,103,382-70,117,671 , GRCh37.p13 chr9: 72,718,298-72,732,587 MAMDC2
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