288895 - dbVar - NCBI

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Number of Variants: 1

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv137444	copy number variation	1	nstd6	human		NCBI35 chr19: 59,917,958-59,917,958 , GRCh37.p13 chr19\|NW_003571060.1: 619,034-619,034 , GRCh37.p13 chr19\|NW_003571061.1: 440,705-440,705 , GRCh37.p13 chr19: 55,226,146-55,226,146 , GRCh37.p13 chr19\|NW_003571054.1: 620,328-620,328 , GRCh38.p12 chr19\|NT_187640.1: 187,972-187,972 , GRCh38.p12 chr19\|NT_187670.1: 168,249-168,249 , GRCh38.p12 chr19\|NT_187673.1: 154,434-154,434 , GRCh38.p12 chr19\|NT_187674.1: 1,487-1,487 , GRCh38.p12 chr19\|NT_187675.1: 13,203-13,203 , GRCh38.p12 chr19\|NT_187686.1: 199,464-199,464 , GRCh38.p12 chr19\|NW_003571054.1: 620,328-620,328 , GRCh38.p12 chr19\|NT_187637.1: 154,132-154,132 , GRCh38.p12 chr19\|NT_187638.1: 140,781-140,781 , GRCh38.p12 chr19\|NT_187643.1: 154,431-154,431 , GRCh38.p12 chr19\|NT_187644.1: 168,232-168,232 , GRCh38.p12 chr19\|NT_187668.1: 188,927-188,927 , GRCh38.p12 chr19\|NT_187687.1: 154,270-154,270 , GRCh38.p12 chr19\|NT_187693.1: 697,260-697,260 , GRCh38.p12 chr19\|NW_003571061.2: 440,706-440,706 , GRCh38.p12 chr19\|NW_003571060.1: 619,034-619,034 , GRCh38.p12 chr19\|NT_187639.1: 154,760-154,760 , GRCh38.p12 chr19\|NT_187641.1: 193,761-193,761 , GRCh38.p12 chr19\|NT_187645.1: 154,413-154,413 , GRCh38.p12 chr19\|NT_187684.1: 184,506-184,506 , GRCh38.p12 chr19\|NT_113949.2: 161,114-161,114 , GRCh38.p12 chr19\|NT_187636.1: 232,540-232,540 , GRCh38.p12 chr19\|NT_187642.1: 139,269-139,269 , GRCh38.p12 chr19\|NT_187669.1: 154,397-154,397 , GRCh38.p12 chr19\|NT_187677.1: 5,633-5,633 , GRCh38.p12 chr19\|NT_187685.1: 153,881-153,881	LILRP2

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Related information

dbSNP
Link from dbVar to dbSNP
Functional Class
Functional class of the sequence domain architecture
Gene
Link from dbVar to Gene
Nucleotide
Link from dbVar to Nucleotide
PubMed
Link from dbVar to PubMed
Taxonomy
Link from dbVar to Taxonomy

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