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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7054895inversion1nstd229human GRCh38 chr2: 229,787,965-232,576,060 , GRCh37.p13 chr2: 230,652,681-233,440,770 GPR55, RN7SL834P, 80 more genes
    nsv6695237copy number variation1nstd229human GRCh38 chr2: 232,362,328-232,544,996 , GRCh37.p13 chr2: 233,227,038-233,409,706 ALPG, CHRND, 9 more genes
    nsv6692763copy number variation1nstd229human GRCh38 chr2: 232,361,901-232,757,800 , GRCh37.p13 chr2: 233,226,611-233,622,510 LOC105373929, CHRND, 16 more genes
    nsv6690553copy number variation1nstd229human GRCh38 chr2: 232,293,780-232,529,812 , GRCh37.p13 chr2: 233,158,490-233,394,522 ECEL1P1, DIS3L2, 10 more genes
    nsv6689075copy number variation1nstd229human GRCh38 chr2: 232,388,792-232,455,618 , GRCh37.p13 chr2: 233,253,502-233,320,328 DIS3L2P1, ECEL1P1, 2 more genes
    nsv6688989copy number variation1nstd229human GRCh38 chr2: 232,273,801-232,522,100 , GRCh37.p13 chr2: 233,138,511-233,386,810 PRSS56, ECEL1P2, 9 more genes
    nsv6688639copy number variation1nstd229human GRCh38 chr2: 232,451,665-232,499,718 , GRCh37.p13 chr2: 233,316,375-233,364,428 ALPI, ECEL1
    nsv6687827copy number variation1nstd229human GRCh38 chr2: 232,460,990-232,471,075 , GRCh37.p13 chr2: 233,325,700-233,335,785 ALPI
    nsv6682306copy number variation1nstd229human GRCh38 chr2: 232,162,461-232,514,393 , GRCh37.p13 chr2: 233,027,171-233,379,103 ECEL1P2, ECEL1P1, 9 more genes
    nsv6628067copy number variation1nstd224human GRCh37 chr2: 233,322,004-233,375,784 , GRCh38.p12 chr2: 232,457,294-232,511,074 ALPI, ECEL1
    nsv6628014copy number variation1nstd224human GRCh37 chr2: 233,204,359-233,321,379 , GRCh38.p12 chr2: 232,339,649-232,456,669 ALPI, ALPP, 7 more genes
    nsv6628013copy number variation1nstd224human GRCh37 chr2: 233,204,359-233,321,089 , GRCh38.p12 chr2: 232,339,649-232,456,379 ALPI, ALPP, 7 more genes
    nsv6628010copy number variation1nstd224human GRCh37 chr2: 233,198,664-233,321,379 , GRCh38.p12 chr2: 232,333,954-232,456,669 ALPI, ALPP, 7 more genes
    nsv6627565copy number variation3nstd224human GRCh37 chr2: 233,215,403-233,321,379 , GRCh38.p12 chr2: 232,350,693-232,456,669 ALPI, ALPP, 5 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LOC105373929, LOC105373932, 204 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 more genes
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