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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5894194copy number variation1nstd209human GRCh38 chr6: 116,748,518-116,750,509 , GRCh37.p13 chr6: 117,069,681-117,071,672 FAM162B
    nsv5843720copy number variation1nstd209human GRCh38 chr6: 116,748,502-116,750,524 , GRCh37.p13 chr6: 117,069,665-117,071,687 FAM162B
    nsv5456529copy number variation1nstd206human GRCh38 chr6: 116,748,521-116,750,510 , GRCh37.p13 chr6: 117,069,684-117,071,673 FAM162B
    nsv5114124mobile element insertion1nstd203human GRCh38 chr6: 116,758,762-116,758,778 , GRCh37.p13 chr6: 117,079,925-117,079,941 FAM162B
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4948358copy number variation1nstd200human GRCh38 chr6: 116,748,521-116,750,510 , GRCh37.p13 chr6: 117,069,684-117,071,673 FAM162B
    nsv4817656copy number variation1nstd200human GRCh37 chr6: 117,069,684-117,071,673 , GRCh38.p12 chr6: 116,748,521-116,750,510 FAM162B
    nsv4768325copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959 GJA1, RNU4-76P, 80 more genes
    nsv4729289copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,978,714-117,537,404 , GRCh38.p12 chr6: 116,657,551-117,216,241 KPNA5, GPRC6A, 6 more genes
    nsv4663193copy number variation1nstd186human GRCh37 chr6: 117,069,681-117,071,673 , GRCh38.p12 chr6: 116,748,518-116,750,510 FAM162B
    nsv4614098copy number variation1nstd183human GRCh37 chr6: 117,069,681-117,071,673 , GRCh38.p12 chr6: 116,748,518-116,750,510 FAM162B
    nsv4493976mobile element insertion1nstd166human GRCh37.p13 chr6: 117,084,671-117,084,671 , GRCh38.p12 chr6: 116,763,508-116,763,508 FAM162B
    nsv4491519mobile element insertion1nstd166human GRCh37.p13 chr6: 117,079,925-117,079,925 , GRCh38.p12 chr6: 116,758,762-116,758,762 FAM162B
    nsv4457007copy number variation1nstd102humanPathogenic GRCh37 chr6: 110,981,075-119,608,396 , GRCh38.p12 chr6: 110,659,872-119,287,231 HDAC2-AS2, NIP7P3, 134 more genes
    nsv4396141copy number variation1nstd174human GRCh37 chr6: 117,069,654-117,071,690 , GRCh38.p12 chr6: 116,748,491-116,750,527 FAM162B
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4312499inversion1nstd166human GRCh37.p13 chr6: 94,532,001-117,422,619 , GRCh38.p12 chr6: 93,822,283-117,101,456 , CRYBG1, 284 more genes
    nsv4143758copy number variation1nstd166human GRCh37.p13 chr6: 117,087,185-117,087,542 , GRCh38.p12 chr6: 116,766,022-116,766,379 LOC105377963, FAM162B
    nsv4137781copy number variation1nstd166human GRCh37.p13 chr6: 117,069,684-117,071,673 , GRCh38.p12 chr6: 116,748,521-116,750,510 FAM162B
    nsv3967095copy number variation1nstd168human GRCh38 chr6: 116,748,511-116,770,717 , GRCh37.p13 chr6: 117,069,674-117,091,880 FAM162B, LOC105377963
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