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Items: 1 to 20 of 707

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113228mobile element insertion1nstd186human GRCh37 chr11: 90,051,816-90,051,816 , GRCh38.p12 chr11|NW_019805497.1: 255,582-255,582 , GRCh38.p12 chr11: 90,318,648-90,318,648 DISC1FP1
    nsv5390143copy number variation2nstd186human GRCh37 chr11: 89,893,084-89,893,159 , GRCh38.p12 chr11: 90,159,916-90,159,991 , GRCh38.p12 chr11|NW_019805497.1: 66,039-66,114 NAALAD2
    nsv5383849mobile element deletion2nstd186human GRCh37 chr11: 89,932,522-89,932,852 , GRCh38.p12 chr11: 90,199,354-90,199,684 , GRCh38.p12 chr11|NW_019805497.1: 105,477-105,807 CHORDC1
    nsv5345512translocation1nstd200human GRCh37 chr11: 90,085,172-90,085,172 , GRCh37 chr11: 90,083,673-90,083,673 , GRCh38.p12 chr11: 90,352,004-90,352,004 , GRCh38.p12 chr11|NW_019805497.1: 287,439-287,439 , GRCh38.p12 chr11: 90,350,505-90,350,505 , GRCh38.p12 chr11|NW_019805497.1: 288,938-288,938 DISC1FP1
    nsv4849088copy number variation1nstd200human GRCh37 chr11: 90,050,074-90,050,853 , GRCh38.p12 chr11: 90,316,906-90,317,685 , GRCh38.p12 chr11|NW_019805497.1: 253,840-254,619 DISC1FP1
    nsv4848079copy number variation1nstd200human GRCh37 chr11: 90,015,186-90,071,684 , GRCh38.p12 chr11|NW_019805497.1: 218,952-275,450 , GRCh38.p12 chr11: 90,282,018-90,338,516 TUBAP2, DISC1FP1
    nsv4846105copy number variation1nstd200human GRCh37 chr11: 89,881,757-89,882,837 , GRCh38.p12 chr11: 90,148,589-90,149,669 , GRCh38.p12 chr11|NW_019805497.1: 54,712-55,792 NAALAD2
    nsv4844369copy number variation1nstd200human GRCh37 chr11: 89,893,084-89,893,159 , GRCh38.p12 chr11|NW_019805497.1: 66,039-66,114 , GRCh38.p12 chr11: 90,159,916-90,159,991 NAALAD2
    nsv4842097copy number variation1nstd200human GRCh37 chr11: 89,875,715-89,910,090 , GRCh38.p12 chr11: 90,142,547-90,176,922 , GRCh38.p12 chr11|NW_019805497.1: 48,670-83,045 NAALAD2
    nsv4839234copy number variation1nstd200human GRCh37 chr11: 89,946,377-89,969,874 , GRCh38.p12 chr11: 90,213,209-90,236,706 , GRCh38.p12 chr11|NW_019805497.1: 119,332-142,829 CHORDC1
    nsv4837127copy number variation1nstd200human GRCh37 chr11: 90,055,935-90,056,119 , GRCh38.p12 chr11|NW_019805497.1: 259,701-259,885 , GRCh38.p12 chr11: 90,322,767-90,322,951 DISC1FP1
    nsv4836495copy number variation1nstd200human GRCh37 chr11: 89,851,104-89,854,075 , GRCh38.p12 chr11: 90,117,936-90,120,907 , GRCh38.p12 chr11|NW_019805497.1: 24,059-27,030 0
    nsv4836151copy number variation1nstd200human GRCh37 chr11: 89,877,591-89,877,684 , GRCh38.p12 chr11: 90,144,423-90,144,516 , GRCh38.p12 chr11|NW_019805497.1: 50,546-50,639 NAALAD2
    nsv4834815copy number variation1nstd200human GRCh37 chr11: 89,841,885-89,850,660 , GRCh38.p12 chr11|NW_019805497.1: 14,840-23,615 , GRCh38.p12 chr11: 90,108,717-90,117,492 0
    nsv4832101copy number variation1nstd200human GRCh37 chr11: 90,027,380-90,027,502 , GRCh38.p12 chr11: 90,294,212-90,294,334 , GRCh38.p12 chr11|NW_019805497.1: 231,146-231,268 DISC1FP1
    nsv4830794copy number variation1nstd200human GRCh37 chr11: 89,950,827-90,043,584 , GRCh38.p12 chr11|NW_019805497.1: 123,782-247,350 , GRCh38.p12 chr11: 90,217,659-90,310,416 TUBAP2, CHORDC1, 1 more genes
    nsv4829568copy number variation1nstd200human GRCh37 chr11: 89,852,199-89,906,705 , GRCh38.p12 chr11|NW_019805497.1: 25,154-79,660 , GRCh38.p12 chr11: 90,119,031-90,173,537 NAALAD2
    nsv4774969mobile element deletion1nstd200human GRCh37 chr11: 89,932,522-89,932,852 , GRCh38.p12 chr11: 90,199,354-90,199,684 , GRCh38.p12 chr11|NW_019805497.1: 105,477-105,807 CHORDC1
    nsv4769098insertion1nstd186human GRCh37 chr11: 90,000,500-90,000,500 , GRCh38.p12 chr11: 90,267,332-90,267,332 , GRCh38.p12 chr11|NW_019805497.1: 204,266-204,266 DISC1FP1
    nsv4769040insertion1nstd186human GRCh37 chr11: 89,992,726-89,992,726 , GRCh38.p12 chr11: 90,259,558-90,259,558 , GRCh38.p12 chr11|NW_019805497.1: 165,679-165,679 DISC1FP1
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