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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 AGT, MAP10, 221 more genes
    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
    nsv7048727inversion1nstd229human GRCh38 chr1: 231,257,209-234,326,619 , GRCh37.p13 chr1: 231,392,955-234,462,365 LOC105373171, LINC01744, 44 more genes
    nsv7044310inversion1nstd229human GRCh38 chr1: 230,890,958-235,370,433 , GRCh37.p13 chr1: 231,026,704-235,533,748 TARBP1, LOC105373170, 86 more genes
    nsv6675874copy number variation1nstd229human GRCh38 chr1: 232,900,608-233,617,904 , GRCh37.p13 chr1: 233,036,354-233,753,650 RPS7P3, MAP3K21, 7 more genes
    nsv6672160copy number variation1nstd229human GRCh38 chr1: 233,336,831-233,341,831 , GRCh37.p13 chr1: 233,472,577-233,477,577 MAP3K21
    nsv6670371copy number variation1nstd229human GRCh38 chr1: 233,375,107-233,424,618 , GRCh37.p13 chr1: 233,510,853-233,560,364 MAP3K21
    nsv6664876copy number variation1nstd229human GRCh38 chr1: 233,375,156-233,389,530 , GRCh37.p13 chr1: 233,510,902-233,525,276 MAP3K21
    nsv6659899copy number variation1nstd229human GRCh38 chr1: 233,341,936-233,344,850 , GRCh37.p13 chr1: 233,477,682-233,480,596 MAP3K21
    nsv6637109copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,895,447-238,787,061 , GRCh38.p12 chr1: 232,759,701-238,623,761 RPL9P10, LOC105373207, 105 more genes
    nsv6637070copy number variation1nstd102humanUncertain significance GRCh37 chr1: 233,120,053-233,572,283 , GRCh38.p12 chr1: 232,984,307-233,436,537 MAP3K21, RPS7P3, 2 more genes
    nsv6637037copy number variation1nstd102humanUncertain significance GRCh37 chr1: 232,827,966-240,750,334 , GRCh38.p12 chr1: 232,692,220-240,587,034 RNU1-74P, EDARADD, 123 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
    nsv6636217copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914 LINC01347, LOC100130331, 169 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
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 OR2M4, KIF28P, 316 more genes
    nsv6625984copy number variation1nstd224human GRCh37 chr1: 233,010,053-233,775,512 , GRCh38.p12 chr1: 232,874,307-233,639,766 LOC105373201, LOC107985361, 8 more genes
    nsv6330555copy number variation1nstd223human GRCh38 chr1: 233,363,714-233,367,870 , GRCh37.p13 chr1: 233,499,460-233,503,616 MAP3K21
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