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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099266copy number variation1nstd231human GRCh38.p12 chr1: 226,993,371-235,936,592 , GRCh37 chr1: 227,181,072-236,099,892 ACTA1, AGT, 223 more genes
    nsv7093371copy number variation1nstd102humannot provided GRCh37 chr1: 224,230,307-243,181,599 , GRCh38.p12 chr1: 224,042,605-243,018,297 RPL36P6, MTND4LP21, 377 more genes
    nsv6677602copy number variation1nstd229human GRCh38 chr1: 228,352,871-228,417,146 , GRCh37.p13 chr1: 228,540,572-228,604,847 TRIM11, MIR6742, 3 more genes
    nsv6673619copy number variation1nstd229human GRCh38 chr1: 228,415,391-228,542,749 , GRCh37.p13 chr1: 228,603,092-228,730,450 H3-4, TRIM17, 8 more genes
    nsv6670489copy number variation1nstd229human GRCh38 chr1: 227,575,489-231,747,964 , GRCh37.p13 chr1: 227,763,190-231,883,710 FAM89A, RNA5S14, 127 more genes
    nsv6668439copy number variation1nstd229human GRCh38 chr1: 228,005,301-228,416,300 , GRCh37.p13 chr1: 228,193,002-228,604,001 LOC101927401, GUK1, 16 more genes
    nsv6665177copy number variation1nstd229human GRCh38 chr1: 228,405,101-228,406,900 , GRCh37.p13 chr1: 228,592,802-228,594,601 TRIM11, TRIM17
    nsv6663744copy number variation1nstd229human GRCh38 chr1: 228,275,386-228,715,659 , GRCh37.p13 chr1: 228,463,087-228,851,406 RNA5S5, H2BC27P, 34 more genes
    nsv6658608copy number variation1nstd229human GRCh38 chr1: 228,413,652-228,449,286 , GRCh37.p13 chr1: 228,601,353-228,636,987 TRIM17, RPL23AP15, 1 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636794copy number variation1nstd102humanPathogenic GRCh37 chr1: 223,972,939-249,224,684 , GRCh38.p12 chr1: 223,785,237-248,930,485 SEPTIN7P13, WNT3A, 546 more genes
    nsv6636265copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 227,992,928-236,659,905 , GRCh38.p12 chr1: 227,805,227-236,496,605 ACTA1, AGT, 211 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6626177copy number variation1nstd224human GRCh37 chr1: 228,553,826-228,824,972 , GRCh38.p12 chr1: 228,366,125-228,689,225 , GRCh38.p12 chr1|NW_018654708.1: 1-266,227 TRIM17, H2BC26, 34 more genes
    nsv6321189copy number variation1nstd223human GRCh38 chr1: 228,336,437-228,544,098 , GRCh37.p13 chr1: 228,524,138-228,731,799 H2BC26, H2BC27P, 12 more genes
    nsv6313841copy number variation1nstd102humanPathogenic GRCh37 chr1: 228,214,912-231,483,538 , GRCh38.p12 chr1: 228,027,211-231,347,792 ISCA1P2, LOC100288703, 105 more genes
    nsv6313700copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 226,131,690-231,908,227 , GRCh38.p12 chr1: 225,943,990-231,772,481 ACTA1, PARP1, 167 more genes
    nsv6290630copy number variation1nstd102humanLikely benign GRCh37 chr1: 228,439,893-228,716,927 , GRCh38.p12 chr1: 228,252,192-228,529,226 RPL23AP15, MIR4666A, 12 more genes
    nsv6290198copy number variation1nstd102humanUncertain significance GRCh37 chr1: 227,782,268-229,506,509 , GRCh38.p12 chr1: 227,594,567-229,370,762 BTNL10P, TRIM17, 70 more genes
    nsv6241075mobile element insertion1nstd215human GRCh38 chr1: 228,406,905-228,406,905 , GRCh37.p13 chr1: 228,594,606-228,594,606 TRIM11, TRIM17
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