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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095981copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,827,745-235,827,941 , GRCh38.p12 chr1: 235,664,445-235,664,641 LYST
    nsv7095593copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 235,850,229-235,860,592 , GRCh38.p12 chr1: 235,686,929-235,697,292 LYST
    nsv5673324copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 235,950,490-235,964,407 , GRCh38.p12 chr1: 235,787,190-235,801,107 LYST
    nsv3887991copy number variation1nstd102humannot provided GRCh38 chr1: 235,728,076-235,728,131 , GRCh37.p13 chr1: 235,891,376-235,891,431 LYST
    nsv6310795copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,826,240-235,976,381 , GRCh38.p12 chr1: 235,662,940-235,813,081 LYST, LDHAP2
    nsv4681654copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,826,220-235,945,407 , GRCh38.p12 chr1: 235,662,920-235,782,107 LYST, LDHAP2
    nsv7095980copy number variation1nstd102humanUncertain significance GRCh37 chr1: 235,826,240-235,945,407 , GRCh38.p12 chr1: 235,662,940-235,782,107 LYST, LDHAP2
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 LYST, OR2M4, 316 more genes
    nsv3904200copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,106,271-243,677,283 , NCBI36 chr1: 228,308,641-241,907,208 , GRCh37 chr1: 230,242,018-243,840,585 LYST, MIR3123, 221 more genes
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 LYST, AGT, 221 more genes
    nsv3876145copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,797,384-249,224,684 , GRCh38.p12 chr1: 235,634,084-248,930,485 LYST, OR11L1, 257 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 LYST, RNU6-747P, 172 more genes
    nsv6636217copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,732,121-243,338,216 , GRCh38.p12 chr1: 232,596,375-243,174,914 LYST, LINC01347, 169 more genes
    nsv3912845copy number variation1nstd102humanPathogenic NCBI36 chr1: 230,713,047-240,722,962 , GRCh37.p13 chr1: 232,646,424-242,656,339 , GRCh38.p12 chr1: 232,510,678-242,493,037 LYST, RNU4-77P, 158 more genes
    nsv3881799copy number variation1nstd102humanPathogenic GRCh37 chr1: 232,226,609-241,010,904 , GRCh38.p12 chr1: 232,090,863-240,847,604 LYST, MIPEPP2, 137 more genes
    nsv3889025copy number variation1nstd102humanPathogenic GRCh37 chr1: 234,605,553-240,932,205 , GRCh38.p12 chr1: 234,469,807-240,768,905 LYST, MIR4428, 102 more genes
    nsv6112661copy number variation1nstd102humanPathogenic GRCh37 chr1: 231,407,943-237,289,859 , GRCh38.p12 chr1: 231,272,197-237,126,559 LYST, LOC105373207, 113 more genes
    nsv4346874copy number variation1nstd102humanPathogenic GRCh37 chr1: 234,742,890-239,475,761 , GRCh38.p12 chr1: 234,607,144-239,312,461 LYST, LINC01348, 82 more genes
    nsv4674008copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,843,930-237,971,511 , GRCh38.p12 chr1: 233,708,184-237,808,211 LYST, LGALS8-AS1, 75 more genes
    nsv7137173copy number variation1nstd102humanPathogenic GRCh38 chr1: 233,502,994-236,105,019 , GRCh37.p13 chr1: 233,638,740-236,268,319 LYST, ARID4B, 58 more genes
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