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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
    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
    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
    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
    nsv6137334translocation1nstd213human GRCh38.p12 chr2: 98,592,478-98,592,478 , GRCh38.p12 chr2: 232,538,161-232,538,161 , GRCh37 chr2: 99,208,941-99,208,941 , GRCh37 chr2: 233,402,871-233,402,871 CHRND, CHRNG, 1 more genes
    nsv6134450copy number variation1nstd213human GRCh37 chr2: 233,390,000-233,500,001 , GRCh38.p12 chr2: 232,525,290-232,635,291 CHRND, CHRNG, 6 more genes
    nsv5551256insertion1nstd206human GRCh38 chr2: 232,539,125-232,539,167 , GRCh37.p13 chr2: 233,403,835-233,403,877 CHRNG
    nsv5351205translocation1nstd200human GRCh38 chr2: 232,536,416-232,536,416 , GRCh38 chr2: 232,539,978-232,539,978 , GRCh37.p13 chr2: 233,404,688-233,404,688 , GRCh37.p13 chr2: 233,401,126-233,401,126 CHRNG, CHRND
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
    nsv4728725copy number variation1nstd102humanPathogenic GRCh37 chr2: 178,397,959-243,007,457 , GRCh38.p12 chr2: 177,533,231-242,065,306 LOC105376755, FZD7, 1013 more genes
    nsv4673913copy number variation1nstd102humanPathogenic GRCh37 chr2: 230,814,690-242,783,384 , GRCh38.p12 chr2: 229,949,974-241,841,232 MIR2467, D2HGDH, 270 more genes
    nsv4543420insertion1nstd166human GRCh37.p13 chr2: 233,403,809-233,403,809 , GRCh38.p12 chr2: 232,539,099-232,539,099 CHRNG
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