Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv508947 | Chr1:16909817 - 17011115 on Build GRCh38 | Insertion | MFAP2 ATP13A2 CROCC |
nsv954854 | Chr1:16961106 - 17013905 on Build GRCh38 | Deletion | MFAP2 ATP13A2 CROCC |
nsv428421 | Chr1:16437838 - 17157486 on Build GRCh38 | Gain+Loss | PADI2 SPATA21 RNU1-1 RNU1-4 MIR3675 RNU1-3 LOC102723383 CROCC MST1P2 MST1L SDHB LOC105376796 LOC105376805 FAM231B NECAP2 FAM231A ESPNP RNU1-2 LOC100132147 MFAP2 CROCCP3 CROCCP2 NBPF1 ATP13A2 |
dgv108n100 | Chr1:16850538 - 17010370 on Build GRCh38 | Gain | LOC105376805 MIR3675 RNU1-2 MFAP2 ATP13A2 CROCC |
dgv92n100 | Chr1:16684943 - 17003642 on Build GRCh38 | Gain | MST1L LOC105376805 ESPNP RNU1-4 MIR3675 RNU1-2 MFAP2 ATP13A2 LOC102723383 CROCC |
nsv834280 | Chr1:16888218 - 17123006 on Build GRCh38 | Loss | PADI2 SDHB LOC105376805 RNU1-2 MFAP2 ATP13A2 CROCC |
nsv834269 | Chr1:16855283 - 17038531 on Build GRCh38 | Loss | SDHB LOC105376805 MIR3675 RNU1-2 MFAP2 ATP13A2 CROCC |