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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099197copy number variation1nstd231human GRCh38.p12 chr1: 43,487,884-44,020,389 , GRCh37 chr1: 43,953,555-44,486,061 ATP6V0B, DPH2, 14 more genes
    nsv6650229copy number variation1nstd229human GRCh38 chr1: 43,707,284-43,713,226 , GRCh37.p13 chr1: 44,172,955-44,178,897 ST3GAL3, ST3GAL3-AS1, 1 more genes
    nsv6650228copy number variation1nstd229human GRCh38 chr1: 43,699,713-43,809,551 , GRCh37.p13 chr1: 44,165,384-44,275,222 KDM4A-AS1, ST3GAL3-AS1, 2 more genes
    nsv6650226copy number variation1nstd229human GRCh38 chr1: 43,558,329-43,714,438 , GRCh37.p13 chr1: 44,024,000-44,180,109 KDM4A-AS1, ST3GAL3, 3 more genes
    nsv6650223copy number variation1nstd229human GRCh38 chr1: 43,490,601-43,889,800 , GRCh37.p13 chr1: 43,956,272-44,355,472 SHMT1P1, KDM4A-AS1, 5 more genes
    nsv6649711copy number variation1nstd229human GRCh38 chr1: 43,707,236-43,707,301 , GRCh37.p13 chr1: 44,172,907-44,172,972 ST3GAL3, KDM4A-AS1
    nsv6636253copy number variation1nstd102humanUncertain significance GRCh37 chr1: 44,115,963-44,434,808 , GRCh38.p12 chr1: 43,650,292-43,969,136 KDM4A, DPH2, 9 more genes
    nsv6329133copy number variation1nstd223human GRCh38 chr1: 43,701,909-43,702,459 , GRCh37.p13 chr1: 44,167,580-44,168,130 KDM4A-AS1, KDM4A
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6139032copy number variation1nstd206human GRCh38 chr1: 43,635,835-43,707,835 , GRCh37.p13 chr1: 44,101,506-44,173,506 ST3GAL3, KDM4A-AS1, 2 more genes
    nsv6133871copy number variation1nstd213human GRCh37 chr1: 44,070,000-46,570,001 , GRCh38.p12 chr1: 43,604,329-46,104,329 ATP6V0B, PLK3, 87 more genes
    nsv4767860inversion1nstd199human GRCh37 chr1: 17,051,740-234,912,187 , GRCh38.p12 chr1: 16,725,245-234,776,440 , ABCA4, 4269 more genes
    nsv4761183inversion1nstd199human GRCh37 chr1: 16,884,570-145,374,569 , GRCh38.p12 chr1: 16,558,075-149,528,945 , ABCA4, 2341 more genes
    nsv4751400inversion1nstd199human GRCh37 chr1: 17,125,657-234,919,132 , GRCh38.p12 chr1: 16,799,162-234,783,385 , ABCA4, 4264 more genes
    nsv4518111copy number variation1nstd166human GRCh37.p13 chr1: 44,172,278-44,172,380 , GRCh38.p12 chr1: 43,706,607-43,706,709 KDM4A-AS1, ST3GAL3
    nsv4453812copy number variation1nstd102humanUncertain significance GRCh37 chr1: 43,787,578-44,221,212 , GRCh38.p12 chr1: 43,321,907-43,755,541 CDC20, MED8, 16 more genes
    nsv4451506copy number variation1nstd102humanPathogenic GRCh37 chr1: 43,336,799-44,713,202 , GRCh38.p12 chr1: 42,871,128-44,247,530 CCDC24, KRT8P47, 54 more genes
    nsv4436181copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,333,430-103,467,088 , GRCh38.p12 chr1: 10,273,372-103,001,532 LINC01776, IGSF21-AS1, 1853 more genes
    nsv4326932inversion1nstd166human GRCh37.p13 chr1: 35,173,490-93,458,530 , GRCh38.p12 chr1: 34,707,889-92,992,973 , ATP6V0B, 1069 more genes
    nsv3900473copy number variation1nstd102humanPathogenic GRCh38 chr1: 40,693,289-44,514,104 , GRCh37 chr1: 41,158,961-44,979,776 , NCBI36 chr1: 40,931,548-44,752,363 KDM4A, RN7SL326P, 102 more genes
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