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Items: 1 to 20 of 32

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4578690copy number variation1nstd102humanUncertain significance GRCh38 chr19: 1,508,507-1,510,399 , GRCh37 chr19: 1,508,506-1,510,398 ADAMTSL5
    nsv3922151copy number variation1nstd102humanPathogenic NCBI36 chr19: 896,098-1,923,298 , GRCh38 chr19: 945,098-1,972,299 , GRCh37 chr19: 945,098-1,972,298 ADAMTSL5, MIR1909, 58 more genes
    nsv7095264copy number variation1nstd102humanPathogenic GRCh37 chr19: 1,206,913-1,650,247 , GRCh38.p12 chr19: 1,206,914-1,650,248 ADAMTSL5, NDUFS7, 30 more genes
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ADAMTSL5, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 ADAMTSL5, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 ADAMTSL5, LENG8, 2408 more genes
    nsv3924102copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-6,795,611 , GRCh37 chr19: 259,395-6,795,622 , NCBI36 chr19: 210,395-6,746,622 ADAMTSL5, POLR2E, 283 more genes
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 ADAMTSL5, BSG, 217 more genes
    nsv3923561copy number variation1nstd102humanPathogenic NCBI36 chr19: 184,565-4,650,484 , GRCh37 chr19: 233,565-4,699,484 , GRCh38 chr19: 233,565-4,699,472 ADAMTSL5, DAPK3, 214 more genes
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 ADAMTSL5, MRPL54, 198 more genes
    nsv4676346copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,501,271 , GRCh38.p12 chr19: 260,911-3,501,273 ADAMTSL5, AZU1, 159 more genes
    nsv3909324copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-3,200,875 , GRCh38.p12 chr19: 260,911-3,200,877 ADAMTSL5, LOC105372234, 152 more genes
    nsv3921932copy number variation1nstd102humanPathogenic NCBI36 chr19: 210,395-2,506,147 , GRCh37 chr19: 259,395-2,555,147 , GRCh38 chr19: 259,395-2,555,149 ADAMTSL5, GZMM, 129 more genes
    nsv3895304copy number variation1nstd102humanPathogenic GRCh37 chr19: 277,373-2,555,164 , GRCh38.p12 chr19: 277,373-2,555,166 ADAMTSL5, LOC100288123, 129 more genes
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 ADAMTSL5, LOC100420586, 113 more genes
    nsv3910990copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-2,068,507 , NCBI36 chr19: 210,395-2,019,506 , GRCh37 chr19: 259,395-2,068,506 ADAMTSL5, SPMAP2, 102 more genes
    nsv3922550copy number variation1nstd102humanPathogenic GRCh38 chr19: 259,395-1,952,650 , GRCh37 chr19: 259,395-1,952,649 , NCBI36 chr19: 210,395-1,903,649 ADAMTSL5, LOC102723811, 99 more genes
    nsv3918029copy number variation1nstd102humanPathogenic NCBI36 chr19: 226,925-1,843,275 , GRCh37 chr19: 275,925-1,892,275 , GRCh38 chr19: 275,925-1,892,276 ADAMTSL5, GPX4, 94 more genes
    nsv3890661copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 259,395-3,152,419 , GRCh38.p12 chr19: 259,395-3,152,421 ADAMTSL5, TLE5, 150 more genes
    nsv3913283copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 372,537-2,848,919 , GRCh37 chr19: 421,537-2,897,919 , GRCh38 chr19: 421,537-2,897,921 ADAMTSL5, AMH, 135 more genes
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