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Items: 1 to 20 of 155

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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
    nsv7096252copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,390,926-233,400,022 , GRCh38.p12 chr2: 232,526,216-232,535,312 PRSS56, CHRND
    nsv7093430delins1nstd102humanPathogenic GRCh37 chr2: 233,394,706-233,394,795 , GRCh38 chr2: 232,529,996-232,530,085 CHRND
    nsv7093163copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,396,141-233,398,358 , GRCh38 chr2: 232,531,431-232,533,648 CHRND
    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
    nsv6693844copy number variation1nstd229human GRCh38 chr2: 232,528,250-232,531,517 , GRCh37.p13 chr2: 233,392,960-233,396,227 CHRND
    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
    nsv6688370copy number variation1nstd229human GRCh38 chr2: 232,537,641-232,543,962 , GRCh37.p13 chr2: 233,402,351-233,408,672 CHRNG, TIGD1, 1 more genes
    nsv6680542copy number variation1nstd229human GRCh38 chr2: 232,528,501-232,531,400 , GRCh37.p13 chr2: 233,393,211-233,396,110 CHRND
    nsv6342835copy number variation1nstd223human GRCh38 chr2: 232,527,725-232,532,437 , GRCh37.p13 chr2: 233,392,435-233,397,147 CHRND
    nsv6341538copy number variation1nstd223human GRCh38 chr2: 232,535,947-232,537,875 , GRCh37.p13 chr2: 233,400,657-233,402,585 CHRNG, CHRND
    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
    nsv6311492copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 233,396,141-233,398,358 , GRCh38.p12 chr2: 232,531,431-232,533,648 CHRND
    nsv6311386copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,164,730-234,250,992 , GRCh38.p12 chr2: 232,300,020-233,342,346 DIS3L2P1, TIGD1, 31 more genes
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