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Items: 1 to 20 of 353

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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
    nsv7094665copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,918,176 , GRCh38.p12 chr16: 206,303-1,868,175 MRPS34, LOC105371044, 97 more genes
    nsv7094664copy number variation1nstd102humanUncertain significance GRCh37 chr16: 256,302-1,843,653 , GRCh38.p12 chr16: 206,303-1,793,652 NME4, UNKL, 94 more genes
    nsv7094663copy number variation2nstd102humanPathogenic GRCh37 chr16: 256,302-1,657,267 , GRCh38.p12 chr16: 206,303-1,607,266 TPSP2, PRR25, 83 more genes
    nsv7094577copy number variation1nstd102humanUncertain significance GRCh37 chr16: 289,853-626,274 , GRCh38.p12 chr16: 239,854-576,274 ARHGDIG, DECR2, 17 more genes
    nsv7094575copy number variation1nstd102humanPathogenic GRCh37 chr16: 256,302-633,035 , GRCh38.p12 chr16: 206,303-583,035 FAM234A, RPL23AP5, 19 more genes
    nsv6965205copy number variation1nstd229human GRCh38 chr16: 275,301-282,200 , GRCh37.p13 chr16: 325,301-332,200 PDIA2, ARHGDIG, 1 more genes
    nsv6962097copy number variation1nstd229human GRCh38 chr16: 122,985-378,594 , GRCh37.p13 chr16: 172,984-428,594 MRPL28, HBA1, 16 more genes
    nsv6960265copy number variation1nstd229human GRCh38 chr16: 159,223-287,986 , GRCh37.p13 chr16: 209,222-337,986 LUC7L, ARHGDIG, 12 more genes
    nsv6959668copy number variation1nstd229human GRCh38 chr16: 237,437-303,730 , GRCh37.p13 chr16: 287,436-353,730 FAM234A, AXIN1, 3 more genes
    nsv6958164copy number variation1nstd229human GRCh38 chr16: 270,771-282,519 , GRCh37.p13 chr16: 320,770-332,519 PDIA2, ARHGDIG, 1 more genes
    nsv6637972copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,881-1,350,186 , GRCh38.p12 chr16: 35,881-1,300,185 MPG, LOC105371038, 78 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
    nsv6623613copy number variation1nstd224human GRCh37 chr16: 337,655-392,485 , GRCh38.p12 chr16: 287,655-342,485 AXIN1, PDIA2
    nsv6623440copy number variation1nstd224human GRCh37 chr16: 295,795-333,339 , GRCh38.p12 chr16: 245,796-283,339 ARHGDIG, PDIA2, 2 more genes
    nsv6623368copy number variation1nstd224human GRCh37 chr16: 138,725-381,927 , GRCh38.p12 chr16: 88,726-331,927 ARHGDIG, HBQ1, 14 more genes
    nsv6314105copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-1,468,828 , GRCh38.p12 chr16: 35,880-1,418,827 HBA2, LUC7L, 87 more genes
    nsv6202826copy number variation1nstd214human GRCh38 chr16: 285,885-285,982 , GRCh37.p13 chr16: 335,885-335,982 PDIA2, AXIN1
    nsv6201610copy number variation1nstd214human GRCh38 chr16: 285,848-285,916 , GRCh37.p13 chr16: 335,848-335,916 AXIN1, PDIA2
    nsv6192174copy number variation1nstd214human GRCh38 chr16: 285,840-286,022 , GRCh37.p13 chr16: 335,840-336,022 AXIN1, PDIA2
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