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Items: 1 to 20 of 266

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5936897copy number variation1nstd209human GRCh38 chr16: 2,238,958-2,239,017 , GRCh37.p13 chr16: 2,288,959-2,289,018 DNASE1L2, ECI1
    nsv5526018copy number variation1nstd206human GRCh38 chr16: 2,238,963-2,239,018 , GRCh37.p13 chr16: 2,288,964-2,289,019 DNASE1L2, ECI1
    nsv5518737copy number variation1nstd206human GRCh38 chr16: 2,219,184-2,241,616 , GRCh37.p13 chr16: 2,269,185-2,291,617 ECI1, E4F1, 1 more genes
    nsv5380995copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,098,597-2,550,979 , GRCh38.p12 chr16: 2,048,596-2,500,978 TEDC2, MIR3677HG, 33 more genes
    nsv5349412translocation1nstd200human GRCh38 chr16: 2,238,963-2,238,963 , GRCh38 chr16: 2,239,018-2,239,018 , GRCh37.p13 chr16: 2,288,964-2,288,964 , GRCh37.p13 chr16: 2,289,019-2,289,019 ECI1, DNASE1L2
    nsv5343874translocation1nstd200human GRCh37 chr16: 2,288,964-2,288,964 , GRCh37 chr16: 2,289,019-2,289,019 , GRCh38.p12 chr16: 2,239,018-2,239,018 , GRCh38.p12 chr16: 2,238,963-2,238,963 ECI1, DNASE1L2
    nsv5325240translocation1nstd204human GRCh37.p13 chr16: 2,289,019-2,289,019 , GRCh37.p13 chr16: 2,288,964-2,288,964 , GRCh38.p13 chr16: 2,239,018-2,239,018 , GRCh38.p13 chr16: 2,238,963-2,238,963 ECI1, DNASE1L2
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5266471copy number variation1nstd204human GRCh38.p13 chr16: 1,936,501-2,552,200 , GRCh37.p13 chr16: 1,986,502-2,602,201 AMDHD2, MIR3178, 56 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5007913copy number variation1nstd200human GRCh38 chr16: 2,238,245-2,238,520 , GRCh37.p13 chr16: 2,288,246-2,288,521 ECI1, DNASE1L2
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4716573copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,157,801-2,288,100 , GRCh38.p12 chr16: 2,107,800-2,238,099 MIR3180-5, BRICD5, 12 more genes
    nsv4682518copy number variation1nstd102humanUncertain significance GRCh37 chr16: 624,055-2,550,979 , GRCh38.p12 chr16: 574,055-2,500,978 C1QTNF8, NHERF2, 133 more genes
    nsv4669080copy number variation1nstd186human GRCh37 chr16: 2,269,304-2,291,605 , GRCh38.p12 chr16: 2,219,303-2,241,604 ECI1, DNASE1L2, 1 more genes
    nsv4624133copy number variation1nstd183human GRCh37 chr16: 2,269,304-2,291,605 , GRCh38.p12 chr16: 2,219,303-2,241,604 E4F1, DNASE1L2, 1 more genes
    nsv4457206copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,070,917-2,592,737 , GRCh38.p12 chr16: 2,020,916-2,542,736 CEMP1, MIR3180-5, 41 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4430371copy number variation1nstd174human GRCh37 chr16: 2,259,191-2,294,890 , GRCh38.p12 chr16: 2,209,190-2,244,889 ECI1, DNASE1L2, 4 more genes
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