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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094683copy number variation1nstd102humanUncertain significance GRCh37 chr16: 65,821,800-72,146,396 , GRCh38.p12 chr16: 65,787,897-72,112,497 TRG-GCC5-1, RNU6-359P, 205 more genes
    nsv7075084inversion1nstd229human GRCh38 chr16: 67,127,296-73,957,488 , GRCh37.p13 chr16: 67,161,199-73,991,387 MIR1538, LINC02136, 187 more genes
    nsv7058675inversion1nstd229human GRCh38 chr16: 67,667,666-75,720,241 , GRCh37.p13 chr16: 67,701,569-75,754,139 RNU6-898P, DPEP2, 199 more genes
    nsv6979644copy number variation1nstd229human GRCh38 chr16: 67,714,195-67,714,262 , GRCh37.p13 chr16: 67,748,098-67,748,165 GFOD2
    nsv6978989copy number variation1nstd229human GRCh38 chr16: 67,641,701-67,678,100 , GRCh37.p13 chr16: 67,675,604-67,712,003 ACD, PARD6A, 4 more genes
    nsv6586736inversion1nstd223human GRCh38 chr16: 67,705,872-67,706,377 , GRCh37.p13 chr16: 67,739,775-67,740,280 GFOD2
    nsv6510901copy number variation1nstd223human GRCh38 chr16: 67,692,994-67,717,681 , GRCh37.p13 chr16: 67,726,897-67,751,584 GFOD2
    nsv6503916copy number variation1nstd223human GRCh38 chr16: 67,705,755-67,706,842 , GRCh37.p13 chr16: 67,739,658-67,740,745 GFOD2
    nsv6503534copy number variation1nstd223human GRCh38 chr16: 67,696,213-67,696,623 , GRCh37.p13 chr16: 67,730,116-67,730,526 GFOD2
    nsv6314755copy number variation1nstd102humanPathogenic GRCh37 chr16: 46,503,968-90,155,062 , GRCh38.p12 chr16: 46,470,056-90,088,654 ATMIN, ATP6V0D1, 826 more genes
    nsv6190556copy number variation1nstd214human GRCh38 chr16: 67,714,195-67,714,261 , GRCh37.p13 chr16: 67,748,098-67,748,164 GFOD2
    nsv6133200copy number variation1nstd213human GRCh37 chr16: 46,460,000-84,740,001 , GRCh38.p12 chr16: 46,426,088-84,706,395 , AARS1, 674 more genes
    nsv6099121insertion1nstd212human GRCh38 chr16: 67,713,002-67,713,002 , GRCh37.p13 chr16: 67,746,905-67,746,905 GFOD2
    nsv6039508copy number variation1nstd212human GRCh38 chr16: 67,695,608-67,696,086 , GRCh37.p13 chr16: 67,729,511-67,729,989 GFOD2
    nsv5980419copy number variation1nstd102humanPathogenic GRCh37 chr16: 67,628,846-67,813,408 , GRCh38.p12 chr16: 67,594,943-67,779,505 CTCF, PARD6A, 6 more genes
    nsv5944837copy number variation1nstd209human GRCh38 chr16: 67,707,197-67,707,506 , GRCh37.p13 chr16: 67,741,100-67,741,409 GFOD2
    nsv5930646copy number variation1nstd209human GRCh38 chr16: 67,714,195-67,714,261 , GRCh37.p13 chr16: 67,748,098-67,748,164 GFOD2
    nsv5712221mobile element insertion2nstd211human GRCh38 chr16: 67,708,877-67,708,877 , GRCh37.p13 chr16: 67,742,780-67,742,780 GFOD2
    nsv5662870insertion1nstd207human GRCh38 chr16: 67,712,970-67,712,970 , GRCh37.p13 chr16: 67,746,873-67,746,873 GFOD2
    nsv5530245copy number variation1nstd206human GRCh38 chr16: 67,687,179-67,687,242 , GRCh37.p13 chr16: 67,721,082-67,721,145 GFOD2
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