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Items: 1 to 20 of 128

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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
    nsv6694974copy number variation1nstd229human GRCh38 chr2: 232,935,882-233,130,889 , GRCh37.p13 chr2: 233,800,592-233,995,599 INPP5D, NEU2, 2 more genes
    nsv6692017copy number variation1nstd229human GRCh38 chr2: 233,014,427-233,019,962 , GRCh37.p13 chr2: 233,879,137-233,884,672 LOC101928881
    nsv6691671copy number variation1nstd229human GRCh38 chr2: 232,868,845-233,267,287 , GRCh37.p13 chr2: 233,733,555-234,175,933 NEU2, LOC101928881, 5 more genes
    nsv6691071copy number variation1nstd229human GRCh38 chr2: 233,013,605-233,022,058 , GRCh37.p13 chr2: 233,878,315-233,886,768 NGEF, LOC101928881
    nsv6683557copy number variation1nstd229human GRCh38 chr2: 232,862,101-233,186,800 , GRCh37.p13 chr2: 233,726,811-234,095,446 INPP5D, NGEF, 3 more genes
    nsv6680019copy number variation1nstd229human GRCh38 chr2: 232,990,748-233,018,140 , GRCh37.p13 chr2: 233,855,458-233,882,850 NGEF, LOC101928881
    nsv6636912copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,642,145-237,654,870 , GRCh38.p12 chr2: 232,777,435-236,746,227 UGT1A, SH3BP4, 70 more genes
    nsv6628015copy number variation1nstd224human GRCh37 chr2: 233,803,391-233,990,592 , GRCh38.p12 chr2: 232,938,681-233,125,882 LOC101928881, NEU2, 2 more genes
    nsv6339681copy number variation1nstd223human GRCh38 chr2: 232,990,748-233,018,137 , GRCh37.p13 chr2: 233,855,458-233,882,847 LOC101928881, NGEF
    nsv6335805copy number variation1nstd223human GRCh38 chr2: 233,014,427-233,019,958 , GRCh37.p13 chr2: 233,879,137-233,884,668 LOC101928881
    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
    nsv6165270copy number variation1nstd214human GRCh38 chr2: 233,015,380-233,015,462 , GRCh37.p13 chr2: 233,880,090-233,880,172 LOC101928881
    nsv6150301copy number variation1nstd214human GRCh38 chr2: 233,014,801-233,014,935 , GRCh37.p13 chr2: 233,879,511-233,879,645 LOC101928881
    nsv5988008copy number variation1nstd212human GRCh38 chr2: 233,015,397-233,015,479 , GRCh37.p13 chr2: 233,880,107-233,880,189 LOC101928881
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