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Items: 1 to 20 of 848

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144381copy number variation1nstd232human GRCh37.p13 chr2: 233,770,885-233,770,933 , GRCh38.p12 chr2: 232,906,175-232,906,223 NGEF
    nsv7143830copy number variation1nstd232human GRCh37.p13 chr2: 233,771,093-233,771,218 , GRCh38.p12 chr2: 232,906,383-232,906,508 NGEF
    nsv7140201copy number variation1nstd232human GRCh37.p13 chr2: 233,765,227-233,765,322 , GRCh38.p12 chr2: 232,900,517-232,900,612 NGEF
    nsv7138355copy number variation1nstd232human GRCh37.p13 chr2: 233,770,806-233,770,854 , GRCh38.p12 chr2: 232,906,096-232,906,144 NGEF
    nsv7137770insertion1nstd232human GRCh37.p13 chr2: 233,750,851-233,750,851 , GRCh38.p12 chr2: 232,886,141-232,886,141 NGEF
    nsv7137192copy number variation1nstd102humanUncertain significance GRCh37 chr2: 232,520,701-234,168,331 , GRCh38.p12 chr2: 231,655,990-233,259,685 NEU2, MIR562, 38 more genes
    nsv6697260copy number variation1nstd229human GRCh38 chr2: 232,836,527-232,894,964 , GRCh37.p13 chr2: 233,701,237-233,759,674 NGEF, GIGYF2, 1 more genes
    nsv6696768copy number variation1nstd229human GRCh38 chr2: 232,935,049-232,936,176 , GRCh37.p13 chr2: 233,799,759-233,800,886 NGEF
    nsv6694974copy number variation1nstd229human GRCh38 chr2: 232,935,882-233,130,889 , GRCh37.p13 chr2: 233,800,592-233,995,599 INPP5D, NEU2, 2 more genes
    nsv6693887copy number variation1nstd229human GRCh38 chr2: 232,954,737-232,960,991 , GRCh37.p13 chr2: 233,819,447-233,825,701 NGEF
    nsv6691671copy number variation1nstd229human GRCh38 chr2: 232,868,845-233,267,287 , GRCh37.p13 chr2: 233,733,555-234,175,933 NEU2, LOC101928881, 5 more genes
    nsv6691267copy number variation1nstd229human GRCh38 chr2: 232,967,438-232,968,237 , GRCh37.p13 chr2: 233,832,148-233,832,947 NGEF
    nsv6691071copy number variation1nstd229human GRCh38 chr2: 233,013,605-233,022,058 , GRCh37.p13 chr2: 233,878,315-233,886,768 NGEF, LOC101928881
    nsv6690939copy number variation1nstd229human GRCh38 chr2: 232,949,638-232,960,304 , GRCh37.p13 chr2: 233,814,348-233,825,014 NGEF
    nsv6689103copy number variation1nstd229human GRCh38 chr2: 233,000,651-233,002,569 , GRCh37.p13 chr2: 233,865,361-233,867,279 NGEF
    nsv6688982copy number variation1nstd229human GRCh38 chr2: 232,968,742-232,988,104 , GRCh37.p13 chr2: 233,833,452-233,852,814 NGEF
    nsv6683766copy number variation1nstd229human GRCh38 chr2: 233,006,331-233,010,042 , GRCh37.p13 chr2: 233,871,041-233,874,752 NGEF
    nsv6683649copy number variation1nstd229human GRCh38 chr2: 232,960,049-232,962,211 , GRCh37.p13 chr2: 233,824,759-233,826,921 NGEF
    nsv6683557copy number variation1nstd229human GRCh38 chr2: 232,862,101-233,186,800 , GRCh37.p13 chr2: 233,726,811-234,095,446 INPP5D, NGEF, 3 more genes
    nsv6683160copy number variation1nstd229human GRCh38 chr2: 232,942,134-232,947,092 , GRCh37.p13 chr2: 233,806,844-233,811,802 NGEF
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