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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094666copy number variation3nstd102humanUncertain significance GRCh37 chr16: 256,302-4,852,572 , GRCh38.p12 chr16: 206,303-4,802,571 DNAAF8, TMEM204, 282 more genes
    nsv6971461copy number variation1nstd229human GRCh38 chr16: 2,259,010-2,260,884 , GRCh37.p13 chr16: 2,309,011-2,310,885 RNPS1
    nsv6958515copy number variation1nstd229human GRCh38 chr16: 2,230,682-2,304,721 , GRCh37.p13 chr16: 2,280,683-2,354,722 ABCA3, MIR3677, 8 more genes
    nsv6637330copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,942,430-2,653,144 , GRCh38.p12 chr16: 1,892,429-2,603,143 SNHG19, SNHG9, 58 more genes
    nsv6634427copy number variation1nstd102humanPathogenic GRCh37 chr16: 111,043-6,627,459 , GRCh38.p12 chr16: 61,045-6,577,458 HBA1, ANTKMT, 312 more genes
    nsv6503466copy number variation1nstd223human GRCh38 chr16: 2,256,387-2,258,952 , GRCh37.p13 chr16: 2,306,388-2,308,953 RNPS1
    nsv6314182copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,847,662-2,653,144 , GRCh38.p12 chr16: 1,797,661-2,603,143 CASKIN1, RPL3L, 63 more genes
    nsv6291471copy number variation1nstd102humanUncertain significance GRCh37 chr16: 1,830,141-2,592,737 , GRCh38.p12 chr16: 1,780,140-2,542,736 CEMP1, NTN3, 65 more genes
    nsv6133285copy number variation1nstd213human GRCh37 chr16: 850,000-2,500,001 , GRCh38.p12 chr16: 800,000-2,450,000 ABCA3, CCNF, 101 more genes
    nsv6133278copy number variation2nstd213human GRCh37 chr16: 60,000-14,990,001 , GRCh38.p12 chr16: 10,001-14,896,144 , ABAT, 446 more genes
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 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
    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
    nsv5155102mobile element insertion1nstd203human GRCh38 chr16: 2,252,139-2,252,154 , GRCh37.p13 chr16: 2,302,140-2,302,155 RNPS1, LOC107984839
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 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
    nsv4627601copy number variation1nstd183human GRCh37 chr16: 2,316,881-2,318,390 , GRCh38.p12 chr16: 2,266,880-2,268,389 MIR3677HG, RNPS1
    nsv4499413mobile element insertion1nstd166human GRCh37.p13 chr16: 2,316,632-2,316,632 , GRCh38.p12 chr16: 2,266,631-2,266,631 RNPS1
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