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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7136949copy number variation1nstd102humanPathogenic GRCh37 chr4: 103,790,345-103,813,965 , GRCh38.p12 chr4: 102,869,188-102,892,808 CISD2, UBE2D3, 1 more genes
    nsv7098788copy number variation1nstd102humanUncertain significance GRCh37 chr4: 101,947,022-107,268,849 , GRCh38.p12 chr4: 101,025,865-106,347,692 LOC107986297, LOC100288914, 60 more genes
    nsv7097220copy number variation1nstd102humanPathogenic GRCh37 chr4: 101,947,022-106,061,534 , GRCh38.p12 chr4: 101,025,865-105,140,377 LOC100419096, LOC105377347, 41 more genes
    nsv7096485copy number variation1nstd102humanPathogenic GRCh37 chr4: 102,001,669-103,806,607 , GRCh38.p12 chr4: 101,080,512-102,885,450 SLC9B1, MIR8066, 24 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7048086inversion1nstd229human GRCh38 chr4: 100,058,481-107,564,371 , GRCh37.p13 chr4: 100,979,638-108,485,528 ACTR6P1, INTS12, 79 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6757951copy number variation1nstd229human GRCh38 chr4: 102,836,249-102,920,311 , GRCh37.p13 chr4: 103,757,406-103,841,468 SLC9B1, PABPC1P7, 4 more genes
    nsv6755725copy number variation1nstd229human GRCh38 chr4: 102,893,225-102,911,964 , GRCh37.p13 chr4: 103,814,382-103,833,121 CISD2, PABPC1P7, 1 more genes
    nsv6753084copy number variation1nstd229human GRCh38 chr4: 102,884,801-102,931,800 , GRCh37.p13 chr4: 103,805,958-103,852,957 SLC9B1, CISD2, 1 more genes
    nsv6744078copy number variation1nstd229human GRCh38 chr4: 102,867,201-102,875,500 , GRCh37.p13 chr4: 103,788,358-103,796,657 CISD2, UBE2D3
    nsv6740568copy number variation1nstd229human GRCh38 chr4: 102,830,147-103,056,103 , GRCh37.p13 chr4: 103,751,304-103,977,260 RNU7-151P, UBE2D3, 6 more genes
    nsv6739590copy number variation1nstd229human GRCh38 chr4: 102,890,806-102,891,234 , GRCh37.p13 chr4: 103,811,963-103,812,391 CISD2, SLC9B1
    nsv6561677inversion1nstd223human GRCh38 chr4: 102,886,215-102,886,772 , GRCh37.p13 chr4: 103,807,372-103,807,929 SLC9B1, CISD2
    nsv6557072inversion1nstd223human GRCh38 chr4: 102,882,200-102,882,770 , GRCh37.p13 chr4: 103,803,357-103,803,927 CISD2
    nsv6394377copy number variation1nstd223human GRCh38 chr4: 102,893,169-102,912,020 , GRCh37.p13 chr4: 103,814,326-103,833,177 SLC9B1, PABPC1P7, 1 more genes
    nsv6380377copy number variation1nstd223human GRCh38 chr4: 102,868,701-102,869,100 , GRCh37.p13 chr4: 103,789,858-103,790,257 CISD2, UBE2D3
    nsv6377356copy number variation1nstd223human GRCh38 chr4: 102,890,806-102,891,234 , GRCh37.p13 chr4: 103,811,963-103,812,391 CISD2, SLC9B1
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